{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\", document_type = \"Rule\" and posted_year = 2021 sorted by posted_date descending", "rows": [["FDA-2018-C-4117-0005", "FDA", "FDA-2018-C-4117", "Listing of Color Additives Exempt\nFrom Certification; Butterfly Pea\nFlower Extract; Confirmation of\nEffective Date", "Rule", "Confirmation of Effective Date", "2021-12-29T05:00:00Z", 2021, 12, "2021-12-29T05:00:00Z", null, "2024-02-08T19:39:46Z", "2021-28158", 0, 0, "0900006484effc3e"], ["FDA-2018-C-4117-0004", "FDA", "FDA-2018-C-4117", "Listing of Color Additives Exempt\nFrom Certification; Butterfly Pea\nFlower Extract; Confirmation of\nEffective Date", "Rule", "Final Rule", "2021-12-29T05:00:00Z", 2021, 12, "2021-12-29T05:00:00Z", null, "2024-02-08T19:39:30Z", "2021-28159", 0, 0, "0900006484effabc"], ["FDA-2021-N-0858-0001", "FDA", "FDA-2021-N-0858", "Medical Devices; Gastroenterology-\nUrology Devices; Classification of the\nTranscutaneous Electrical Continence\nDevice", "Rule", "Final Rule", "2021-12-29T05:00:00Z", 2021, 12, "2021-12-29T05:00:00Z", null, "2021-12-29T17:27:03Z", "2021-28163", 0, 0, "0900006484effb9a"], ["FDA-2021-N-0573-0001", "FDA", "FDA-2021-N-0573", "Medical Devices; Neurological\nDevices; Classification of the\nDiagnostic Neurosurgical Microscope\nFilter", "Rule", "Final Rule", "2021-12-29T05:00:00Z", 2021, 12, "2021-12-29T05:00:00Z", null, "2021-12-29T17:27:59Z", "2021-28160", 0, 0, "0900006484effbf4"], ["FDA-2021-N-0855-0001", "FDA", "FDA-2021-N-0855", "Medical Devices; Neurological\nDevices; Classification of the\nCerebrospinal Fluid Shunt System", "Rule", "Final Rule", "2021-12-29T05:00:00Z", 2021, 12, "2021-12-29T05:00:00Z", null, "2021-12-29T17:26:25Z", "2021-28157", 0, 0, "0900006484effaf3"], ["FDA-2021-N-0917-0001", "FDA", "FDA-2021-N-0917", "Medical Devices; Anesthesiology\nDevices; Classification of the\nRetrograde Intubation Device", "Rule", "Final Rule", "2021-12-28T05:00:00Z", 2021, 12, "2021-12-28T05:00:00Z", null, "2021-12-28T17:42:04Z", "2021-28166", 0, 0, "0900006484efed3f"], ["FDA-2021-N-0857-0001", "FDA", "FDA-2021-N-0857", "Medical Devices; General and Plastic Surgery Devices; Classification of the Manual Percutaneous Surgical Set\nAssembled in the Abdomen", "Rule", "Final Rule", "2021-12-17T05:00:00Z", 2021, 12, "2021-12-17T05:00:00Z", null, "2021-12-21T20:01:33Z", "2021-27317", 0, 0, "0900006484ed1e64"], ["FDA-2021-N-0896-0001", "FDA", "FDA-2021-N-0896", "Medical Devices; Neurological Devices; Classification of the Traumatic Brain Injury Eye Movement Assessment Aid", "Rule", "Final Rule", "2021-12-16T05:00:00Z", 2021, 12, "2021-12-16T05:00:00Z", null, "2021-12-16T15:19:44Z", "2021-27227", 0, 0, "0900006484ecfb05"], ["FDA-2021-N-0583-0001", "FDA", "FDA-2021-N-0583", "Medical Devices; Gastroenterology-\nUrology Devices; Classification of the\nNonimplanted Nerve Stimulator for\nFunctional Abdominal Pain Relief", "Rule", "Final Rule", "2021-12-15T05:00:00Z", 2021, 12, "2021-12-15T05:00:00Z", null, "2021-12-15T16:16:01Z", "2021-27132", 0, 0, "0900006484ecaef9"], ["FDA-2021-N-0590-0001", "FDA", "FDA-2021-N-0590", "Medical Devices; Gastroenterology-\nUrology Devices; Classification of the\nEndoscopic Transhepatic Venous\nAccess Needle", "Rule", "Final Rule", "2021-12-15T05:00:00Z", 2021, 12, "2021-12-15T05:00:00Z", null, "2021-12-15T16:15:11Z", "2021-27135", 0, 0, "0900006484ecae9c"], ["FDA-2021-N-0898-0001", "FDA", "FDA-2021-N-0898", "Medical Devices; Gastroenterology-Urology Devices; Classification of the Pressure Ulcer Management Tool", "Rule", "Final Rule", "2021-12-13T05:00:00Z", 2021, 12, "2021-12-13T05:00:00Z", null, "2021-12-13T14:21:04Z", "2021-26924", 0, 0, "0900006484ec08ac"], ["FDA-2021-N-0575-0001", "FDA", "FDA-2021-N-0575", "Medical Devices; Neurological Devices; Classification of the Temporary Coil Embolization Assist Device", "Rule", "Final Rule", "2021-12-13T05:00:00Z", 2021, 12, "2021-12-13T05:00:00Z", null, "2021-12-13T14:12:28Z", "2021-26926", 0, 0, "0900006484ec0865"], ["FDA-2021-N-0572-0001", "FDA", "FDA-2021-N-0572", "Medical Devices; General and Plastic\nSurgery Devices; Classification of the\nNegative Pressure Wound Therapy\nDevice for Reduction of Wound\nComplications", "Rule", "Final Rule", "2021-12-10T05:00:00Z", 2021, 12, "2021-12-10T05:00:00Z", null, "2021-12-10T15:02:42Z", "2021-26741", 0, 0, "0900006484eb80bc"], ["FDA-2021-N-0585-0001", "FDA", "FDA-2021-N-0585", "Medical Devices; Gastroenterology-Urology Devices; Classification of the Ingested, Transient, Space Occupying Device for Weight Management and/or Weight Loss", "Rule", "Final Rule", "2021-12-10T05:00:00Z", 2021, 12, "2021-12-10T05:00:00Z", null, "2021-12-10T14:34:02Z", "2021-26738", 0, 0, "0900006484eb7ff4"], ["FDA-2021-N-0595-0001", "FDA", "FDA-2021-N-0595", "Medical Devices; Neurological Devices; Classification of the Transcutaneous Electrical Nerve Stimulator for Attention Deficit\nHyperactivity Disorder", "Rule", "Final Rule", "2021-12-10T05:00:00Z", 2021, 12, "2021-12-10T05:00:00Z", null, "2021-12-10T14:39:25Z", "2021-26740", 0, 0, "0900006484eb80b9"], ["FDA-2019-N-3065-0878", "FDA", "FDA-2019-N-3065", "Tobacco Products; Required Warnings for Cigarette Packages and Advertisements; Delayed Effective Date", "Rule", "Delay of Effective Date", "2021-12-09T05:00:00Z", 2021, 12, "2021-12-09T05:00:00Z", null, "2021-12-09T14:21:52Z", "2021-26643", 0, 0, "0900006484eb2301"], ["FDA-2021-P-0424-0007", "FDA", "FDA-2021-P-0424", "Medical Devices; Exemption From Premarket Notification: Powered Patient Transport, All Other Powered Patient Transport", "Rule", "Final Rule", "2021-12-08T05:00:00Z", 2021, 12, "2021-12-08T05:00:00Z", null, "2021-12-08T14:03:54Z", "2021-26636", 0, 0, "0900006484eaede6"], ["FDA-2019-N-3325-0124", "FDA", "FDA-2019-N-3325", "Laboratory Accreditation for Analyses of Foods", "Rule", "Final Rule", "2021-12-03T05:00:00Z", 2021, 12, "2021-12-03T05:00:00Z", null, "2021-12-03T16:37:13Z", "2021-25716", 0, 0, "0900006484e9c71c"], ["FDA-2021-N-0261-0001", "FDA", "FDA-2021-N-0261", "Medical Devices; Neurological Devices; Classification of the Trunk and Limb Electrical Stimulator To Treat Headache", "Rule", "Final Rule", "2021-12-02T05:00:00Z", 2021, 12, "2021-12-02T05:00:00Z", null, "2021-12-02T19:09:34Z", "2021-26175", 0, 0, "0900006484e9360d"], ["FDA-2021-N-0622-0001", "FDA", "FDA-2021-N-0622", "Medical Devices; Anesthesiology Devices; Classification of the Isocapnic Ventilation Device", "Rule", "Final Rule", "2021-12-02T05:00:00Z", 2021, 12, "2021-12-02T05:00:00Z", null, "2021-12-02T19:04:51Z", "2021-26201", 0, 0, "0900006484e935d6"], ["FDA-2021-N-0290-0001", "FDA", "FDA-2021-N-0290", "Medical Devices; Neurological Devices; Classification of the Conditioning Tool for Eating Disorders", "Rule", "Final Rule", "2021-12-02T05:00:00Z", 2021, 12, "2021-12-02T05:00:00Z", null, "2021-12-02T19:14:44Z", "2021-26176", 0, 0, "0900006484e9360f"], ["FDA-2021-N-0648-0001", "FDA", "FDA-2021-N-0648", "Medical Devices; Orthopedic Devices;\nClassification of the Intraoperative\nOrthopedic Strain Sensor", "Rule", "Final Rule", "2021-12-02T05:00:00Z", 2021, 12, "2021-12-02T05:00:00Z", null, "2021-12-02T16:48:33Z", "2021-26183", 0, 0, "0900006484e93613"], ["FDA-2021-N-0285-0001", "FDA", "FDA-2021-N-0285", "Medical Devices; Gastroenterology- Urology Devices; Classification of the Esophageal Tissue Characterization System", "Rule", "Final Rule", "2021-12-02T05:00:00Z", 2021, 12, "2021-12-02T05:00:00Z", null, "2021-12-02T19:26:34Z", "2021-26200", 0, 0, "0900006484e9372d"], ["FDA-2018-N-1913-0001", "FDA", "FDA-2018-N-1913", "Medical Devices; General and Plastic Surgery Devices; Classification of the General Laparoscopic Power Morcellation Containment System", "Rule", "Final Rule", "2021-11-23T05:00:00Z", 2021, 11, "2021-11-23T05:00:00Z", null, "2021-11-23T15:02:19Z", "2021-25585", 0, 0, "0900006484e7590e"], ["FDA-2016-N-0400-0191", "FDA", "FDA-2016-N-0400", "Medical Devices; General and Plastic Surgery Devices; Reclassification of Blood Lancets", "Rule", "Final Rule", "2021-11-22T05:00:00Z", 2021, 11, "2021-11-22T05:00:00Z", null, "2021-11-22T15:51:30Z", "2021-25376", 0, 0, "0900006484e71279"], ["FDA-2016-M-0035-0045", "FDA", "FDA-2016-M-0035", "Effective Date of Requirement for\nPremarket Approval for Blood Lancets", "Rule", "Final Rule", "2021-11-22T05:00:00Z", 2021, 11, "2021-11-22T05:00:00Z", null, "2021-11-22T15:54:18Z", "2021-25381", 0, 0, "0900006484e71390"], ["FDA-2020-N-1088-0014", "FDA", "FDA-2020-N-1088", "Microbiology Devices; Reclassification of Nucleic Acid-Based Hepatitis C Virus Ribonucleic Acid Assay Devices, Renamed to Nucleic Acid-Based Hepatitis C Virus Ribonucleic Acid Tests", "Rule", "Final Rule", "2021-11-22T05:00:00Z", 2021, 11, "2021-11-22T05:00:00Z", null, "2021-11-22T15:44:54Z", "2021-25379", 0, 0, "0900006484e71238"], ["FDA-2020-N-1082-0018", "FDA", "FDA-2020-N-1082", "Microbiology Devices; Reclassification of Certain Hepatitis C Virus Antibody Assay Devices, Renamed to Hepatitis C Virus Antibody Tests", "Rule", "Final Rule", "2021-11-22T05:00:00Z", 2021, 11, "2021-11-22T05:00:00Z", null, "2021-11-22T15:48:14Z", "2021-25374", 0, 0, "0900006484e71277"], ["FDA-2021-N-0002-0024", "FDA", "FDA-2021-N-0002", "New Animal Drugs; Approval of New Animal Drug Applications; Changes of Sponsor Address", "Rule", "Final Rule", "2021-11-08T05:00:00Z", 2021, 11, "2021-11-08T05:00:00Z", null, "2021-11-08T14:01:16Z", "2021-24075", 0, 0, "0900006484e35459"], ["FDA-2021-N-0002-0001", "FDA", "FDA-2021-N-0002", "New Animal Drugs; Approval of New Animal Drug Applications; Changes of Sponsorship", "Rule", "Final Rule", "2021-10-20T04:00:00Z", 2021, 10, "2021-10-20T04:00:00Z", null, "2021-10-20T15:15:02Z", "2021-22604", 0, 0, "0900006484dcea30"], ["FDA-2019-N-1250-0009", "FDA", "FDA-2019-N-1250", "General and Plastic Surgery Devices; Reclassification of Certain Surgical Staplers", "Rule", "Final Rule", "2021-10-08T04:00:00Z", 2021, 10, "2021-10-08T04:00:00Z", null, "2021-10-15T14:13:19Z", "2021-22041", 0, 0, "0900006484dbf9b9"], ["FDA-2017-C-1951-0235", "FDA", "FDA-2017-C-1951", "Termination of Listing of Color\nAdditives Exempt From Certification;\nLead Acetate", "Rule", "Final Rule", "2021-10-08T04:00:00Z", 2021, 10, "2021-10-08T04:00:00Z", null, "2021-10-08T13:20:08Z", "2021-21892", 0, 0, "0900006484dbf0c6"], ["FDA-2018-C-0617-0006", "FDA", "FDA-2018-C-0617", "Listing of Color Additives Exempt From Certification; Silver Nitrate", "Rule", "Final Rule", "2021-10-06T04:00:00Z", 2021, 10, "2021-10-06T04:00:00Z", "2021-11-06T03:59:59Z", "2021-11-05T01:01:00Z", "2021-21755", 0, 0, "0900006484dbc6b8"], ["FDA-2016-N-3818-0176", "FDA", "FDA-2016-N-3818", "Content and Format of Substantial Equivalence Reports; Food and Drug Administration Actions on Substantial Equivalence Reports", "Rule", "Final Rule", "2021-10-05T04:00:00Z", 2021, 10, "2021-10-05T04:00:00Z", null, "2021-10-05T20:23:28Z", "2021-21009", 0, 0, "0900006484dba96e"], ["FDA-2018-N-0236-0028", "FDA", "FDA-2018-N-0236", "Medical Device De Novo Classification Process", "Rule", "Final Rule", "2021-10-05T04:00:00Z", 2021, 10, "2021-10-05T04:00:00Z", null, "2021-10-05T16:21:46Z", "2021-21677", 0, 0, "0900006484dbaa56"], ["FDA-2019-N-2854-1147", "FDA", "FDA-2019-N-2854", "Premarket Tobacco Product Applications and Recordkeeping \nRequirements", "Rule", "Final Rule", "2021-10-05T04:00:00Z", 2021, 10, "2021-10-05T04:00:00Z", null, "2021-10-05T20:22:52Z", "2021-21011", 0, 0, "0900006484dba972"], ["FDA-2001-N-0075-0027", "FDA", "FDA-2001-N-0075", "Import Tolerances for Residues of Unapproved New Animal Drugs in \nFood", "Rule", "Final Rule", "2021-09-21T04:00:00Z", 2021, 9, "2021-09-21T04:00:00Z", "2021-10-22T03:59:59Z", "2021-10-22T01:01:24Z", "2021-19967", 0, 0, "0900006484d98dbf"], ["FDA-2019-N-3065-0877", "FDA", "FDA-2019-N-3065", "Tobacco Products; Required Warnings for Cigarette Packages and Advertisements; Delayed Effective Date", "Rule", "Delay of Effective Date", "2021-09-13T04:00:00Z", 2021, 9, "2021-09-13T04:00:00Z", null, "2022-06-01T13:02:06Z", "2021-19688", 0, 0, "0900006484d75ac6"], ["FDA-2021-N-0011-0001", "FDA", "FDA-2021-N-0011", "Revision to Restrictions on Shipment or Use for Human Blood and Blood Components Exceptions; Technical Amendment", "Rule", "Final Rule", "2021-09-07T04:00:00Z", 2021, 9, "2021-09-07T04:00:00Z", null, "2021-09-07T13:10:03Z", "2021-19220", 0, 0, "0900006484d56736"], ["FDA-2018-C-4117-0002", "FDA", "FDA-2018-C-4117", "Listing of Color Additives Exempt From Certification; Butterfly Pea Flower Extract", "Rule", "Final Rule", "2021-09-02T04:00:00Z", 2021, 9, "2021-09-02T04:00:00Z", "2021-10-05T03:59:59Z", "2024-02-08T19:39:13Z", "2021-18995", 0, 0, "0900006484d43741"], ["FDA-2015-N-2002-2054", "FDA", "FDA-2015-N-2002", "Regulations Regarding \u2018\u2018Intended Uses\u2019\u2019", "Rule", "Final Rule", "2021-08-02T04:00:00Z", 2021, 8, "2021-08-02T04:00:00Z", null, "2021-08-02T16:56:29Z", "2021-15980", 0, 0, "0900006484c2027a"], ["FDA-2020-F-1289-0002", "FDA", "FDA-2020-F-1289", "Food Additives Permitted in Feed and Drinking Water of Animals; Selenomethionine Hydroxy Analogue", "Rule", "Final Rule", "2021-07-14T04:00:00Z", 2021, 7, "2021-07-14T04:00:00Z", "2021-08-14T03:59:59Z", "2021-07-20T17:26:00Z", "2021-15072", 0, 0, "0900006484befa85"], ["FDA-2019-F-5401-0002", "FDA", "FDA-2019-F-5401", "Food Additives Permitted in Feed and Drinking Water of Animals; Guanidinoacetic Acid", "Rule", "Final Rule", "2021-07-14T04:00:00Z", 2021, 7, "2021-07-14T04:00:00Z", "2021-08-14T03:59:59Z", "2021-07-15T01:00:26Z", "2021-15070", 0, 0, "0900006484befa35"], ["FDA-2019-N-3065-0876", "FDA", "FDA-2019-N-3065", "Tobacco Products; Required Warnings for Cigarette Packages and Advertisements; Delayed Effective Date", "Rule", "Delay of Effective Date", "2021-07-12T04:00:00Z", 2021, 7, "2021-07-12T04:00:00Z", null, "2021-07-12T15:35:12Z", "2021-14678", 0, 0, "0900006484be4280"], ["FDA-2000-P-0126-0096", "FDA", "FDA-2000-P-0126", "Milk and Cream Products and Yogurt Products; Final Rule To Revoke the Standards for Lowfat Yogurt and\nNonfat Yogurt and To Amend the Standard for Yogurt", "Rule", "Final Rule", "2021-06-11T04:00:00Z", 2021, 6, "2021-06-11T04:00:00Z", "2021-07-13T03:59:59Z", "2023-05-19T12:29:26Z", "2021-12220", 0, 0, "0900006484b6bc96"], ["FDA-2018-N-1440-0001", "FDA", "FDA-2018-N-1440", "Medical Devices; Medical Device Classification Regulations To Conform  to Medical Software Provisions in the  21st Century Cures Act", "Rule", "Final Rule", "2021-04-19T04:00:00Z", 2021, 4, "2021-04-19T04:00:00Z", null, "2021-04-19T18:10:31Z", "2021-07860", 0, 0, "0900006484aab448"], ["FDA-2021-N-0246-0001", "FDA", "FDA-2021-N-0246", "Medical Devices; Technical Amendments", "Rule", "Final Rule", "2021-04-01T04:00:00Z", 2021, 4, "2021-04-01T04:00:00Z", null, "2023-03-21T15:12:01Z", "2021-06681", 0, 0, "0900006484a9351a"], ["FDA-2016-N-1487-0024", "FDA", "FDA-2016-N-1487", "Electronic Import Entries; Technical Amendments", "Rule", "Final Rule", "2021-04-01T04:00:00Z", 2021, 4, "2021-04-01T04:00:00Z", null, "2021-04-01T17:01:37Z", "2021-06679", 0, 0, "0900006484a92f39"], ["FDA-2005-N-0464-0249", "FDA", "FDA-2005-N-0464", "Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated Under a Biologics License Application, and Animal Drugs; 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