{"database": "openregs", "table": "documents", "rows": [["FDA-2011-D-0476-0001", "FDA", "FDA-2011-D-0476", "Draft Guidance for Industry and Food and Drug Administration Staff: Enforcement Policy for Premarket Notification Requirements for Certain In Vitro Diagnostic and Radiology Devices", "Notice", "Notice of Availability", "2011-07-12T04:00:00Z", 2011, 7, "2011-07-12T04:00:00Z", "2011-10-12T03:59:59Z", "2011-10-12T20:38:43Z", "2011-17352", 0, 0, "0900006480ec0678"]], "columns": ["id", "agency_id", "docket_id", "title", "document_type", "subtype", "posted_date", "posted_year", "posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2011-D-0476-0001"], "units": {}, "query_ms": 49.38497603870928, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}