{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\" and docket_id = \"FDA-2009-N-0664\" sorted by posted_date descending", "rows": [["FDA-2009-N-0664-0136", "FDA", "FDA-2009-N-0664", "Cardiovascular and Renal Drugs Advisory Committee; Notice of Meeting", "Notice", "NM-Notice of Meeting", "2010-01-11T05:00:00Z", 2010, 1, null, null, "2010-01-20T04:11:31Z", "2010-00173", 0, 0, "0900006480a7b2e4"], ["FDA-2009-N-0664-0135", "FDA", "FDA-2009-N-0664", "The General Hospital and Personal Use Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting", "Notice", "NM-Notice of Meeting", "2010-01-11T05:00:00Z", 2010, 1, null, null, "2010-01-20T04:11:31Z", "2010-00174", 0, 0, "0900006480a7b2a5"], ["FDA-2009-N-0664-0134", "FDA", "FDA-2009-N-0664", "Anesthetic and Life Support Drugs Advisory Committee; Cancellation", "Notice", "N-Notice", "2010-01-06T05:00:00Z", 2010, 1, null, null, "2010-01-06T12:57:43Z", "E9-31306", 0, 0, "0900006480a7791a"], ["FDA-2009-N-0664-0133", "FDA", "FDA-2009-N-0664", "Public Workshop: Medical Device Quality System Regulation Educational Forum on Risk Management Through the Product Life Cycle", "Notice", "NM-Notice of Meeting", "2010-01-05T05:00:00Z", 2010, 1, null, null, "2010-01-05T14:05:54Z", "E9-31198", 0, 0, "0900006480a76f8b"], ["FDA-2009-N-0664-0131", "FDA", "FDA-2009-N-0664", "Medical Device Interoperability; 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