{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\" and posted_year = 2000 sorted by posted_date descending", "rows": [["FDA-2000-P-0151-0001", "FDA", "FDA-2000-P-0151", "FDA/DDM to Satori Food Corp.", "Other", "ACK-Acknowledgement Letter", "2000-12-29T05:00:00Z", 2000, 12, null, null, "2008-04-25T01:31:51Z", null, 0, 0, "09000064804d117d"], ["FDA-2000-N-0039-0001", "FDA", "FDA-2000-N-0039", "Agency Information Collection Activities; Proposed Collection; Comment Request; Shipment of a Blood Product Prior to Completion of Testing for Hepatitis B Surface Antigen (HBsAg); and Shipment of Blood Products Known Reactive for HBsAg", "Notice", "General Notice", "2000-12-28T05:00:00Z", 2000, 12, "2000-09-07T04:00:00Z", "2000-11-07T04:59:59Z", "2025-06-12T20:27:59Z", "00-22951", 0, 0, "09000064804aeef1"], ["FDA-2000-N-0044-0001", "FDA", "FDA-2000-N-0044", "Requirements on Content and Format of Labeling for Human Prescription Drugs and Biologics; 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Availability of Safety and Effectiveness Summaries for PMA", "Notice", "Notice of Data Availability", "2000-12-27T05:00:00Z", 2000, 12, null, null, "2025-07-21T23:25:52Z", "00-31960", 0, 0, "09000064804d23dd"], ["FDA-2000-M-0178-0001", "FDA", "FDA-2000-M-0178", "Medical Devices; Availability of Safety and Effectiveness Summaries for PMA", "Notice", "Notice of Data Availability", "2000-12-27T05:00:00Z", 2000, 12, null, null, "2025-07-21T23:15:54Z", "00-31960", 0, 0, "09000064804d27c8"], ["FDA-2000-M-0117-0001", "FDA", "FDA-2000-M-0117", "Medical Devices; Availability of Safety and Effectiveness Summaries for PMA", "Notice", "Notice of Data Availability", "2000-12-27T05:00:00Z", 2000, 12, null, null, "2025-07-21T22:48:43Z", "00-31960", 0, 0, "09000064804cf1d7"], ["FDA-2000-M-0019-0001", "FDA", "FDA-2000-M-0019", "Medical Devices; Availability of Safety and Effectiveness Summaries for PMA", "Notice", "Notice of Data Availability", "2000-12-27T05:00:00Z", 2000, 12, null, null, "2025-07-09T23:38:44Z", "00-31960", 0, 0, "09000064804ae968"], ["FDA-2000-N-0044-0003", "FDA", "FDA-2000-N-0044", "Requirements on Content and Format of Labeling for Human Prescription Drugs and Biologics; 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Draft Guidance for Industry on Safety Studies for Veterinary Drug Residues in Human Food: Genotoxicity Studies (VICH GL23); Availability; Request for Comments", "Notice", "Notice of Data Availability", "2000-12-18T05:00:00Z", 2000, 12, "2000-12-18T05:00:00Z", "2001-01-18T04:59:59Z", "2013-08-11T04:11:06Z", null, 0, 0, "09000064804dd8b2"], ["FDA-2000-D-0598-0002", "FDA", "FDA-2000-D-0598", "Guidance for Industry #116 Safety Studies for Veterinary Drug Residues in Human Food: Genotoxicity Studies VICH GL23; Draft Guidance", "Other", "Guidance", "2000-12-18T05:00:00Z", 2000, 12, "2013-01-23T05:00:00Z", null, "2013-01-24T03:08:44Z", null, 0, 0, "09000064804dd8b1"], ["FDA-2000-P-0066-0001", "FDA", "FDA-2000-P-0066", "Notice of Final Rule: Medical Device; Exemption From Premarket Notification; Class II Devices; Barium Enema Retention Catheters and Tips With or Without a Bag", "Notice", "Notice of Final Rule", "2000-12-14T05:00:00Z", 2000, 12, null, null, "2026-01-22T22:35:19Z", null, 0, 0, "09000064804afc70"], ["FDA-1997-C-0030-0003", "FDA", "FDA-1997-C-0030", "Listing of Color Additives Exempt From Certification; 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