{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\", document_type = \"Proposed Rule\" and posted_year = 2019 sorted by posted_date descending", "rows": [["FDA-2008-P-0086-0030", "FDA", "FDA-2008-P-0086", "Cheeses and Related CheeseProducts; Proposal To Permit the Use of Ultrafiltered Milk; Reopening the Comment Period", "Proposed Rule", "Reopening of Comment Period", "2019-12-30T05:00:00Z", 2019, 12, "2019-12-30T05:00:00Z", null, "2020-04-15T20:32:35Z", "2019-28145", 0, 0, "0900006484256f2a"], ["FDA-2019-N-5711-0001", "FDA", "FDA-2019-N-5711", "Importation of Prescription Drugs", "Proposed Rule", "Amendment", "2019-12-23T05:00:00Z", 2019, 12, "2019-12-23T05:00:00Z", "2020-03-10T03:59:59Z", "2022-01-18T02:00:13Z", "2019-27474", 0, 0, "090000648424842c"], ["FDA-2019-N-3101-0001", "FDA", "FDA-2019-N-3101", "Revised Procedures for the Announcement of Approvals and Denials of Premarket Approval Applications and Humanitarian Device Exemption Applications", "Proposed Rule", "Amendment", "2019-12-17T05:00:00Z", 2019, 12, "2019-12-17T05:00:00Z", "2020-03-03T04:59:59Z", "2020-03-04T02:02:53Z", "2019-27045", 0, 0, "090000648421ceeb"], ["FDA-2017-F-4399-0010", "FDA", "FDA-2017-F-4399", "Zinpro Corp.; 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Food and Drug Administration Actions on Substantial Equivalence Reports; Extension of Comment Period", "Proposed Rule", "Extension of Comment Period", "2019-06-13T04:00:00Z", 2019, 6, "2019-06-13T04:00:00Z", "2019-07-18T03:59:59Z", "2019-06-13T21:14:01Z", "2019-12478", 0, 0, "0900006483d0d911"], ["FDA-2019-D-0892-0001", "FDA", "FDA-2019-D-0892", "The Use of an Alternate Name for Potassium Chloride in Food Labeling;\nDraft Guidance for Industry; Availability", "Proposed Rule", "GDL Guidance", "2019-05-20T04:00:00Z", 2019, 5, "2019-05-20T04:00:00Z", "2019-07-20T03:59:59Z", "2019-07-11T01:05:50Z", "2019-10401", 0, 0, "0900006483ca0db2"], ["FDA-2019-C-1782-0001", "FDA", "FDA-2019-C-1782", "CooperVision, Inc.; Filing of Color Additive Petition", "Proposed Rule", "Petition", "2019-05-08T04:00:00Z", 2019, 5, "2019-05-08T04:00:00Z", null, "2019-05-08T13:39:36Z", "2019-09411", 0, 0, "0900006483c43a7a"], ["FDA-2019-N-1250-0001", "FDA", "FDA-2019-N-1250", "General and Plastic Surgery Devices; Reclassification of Certain Surgical Staplers", "Proposed Rule", "Amendment", "2019-04-24T04:00:00Z", 2019, 4, "2019-04-24T04:00:00Z", "2019-06-25T03:59:59Z", "2019-06-25T01:01:16Z", "2019-08260", 0, 0, "0900006483be9aa2"], ["FDA-2015-F-0537-0053", "FDA", "FDA-2015-F-0537", "Natural Resources Defense Council et al.: Response to the Objections and Denial of the Requests for a Public Hearing", "Proposed Rule", "Denial", "2019-04-24T04:00:00Z", 2019, 4, "2019-04-24T04:00:00Z", null, "2019-04-24T15:54:26Z", "2019-08262", 0, 0, "0900006483be9aef"], ["FDA-2018-D-2074-0001", "FDA", "FDA-2018-D-2074", "Initiation of Voluntary Recalls Draft Guidance for Industry and Food and Drug Administration Staff; 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