{"database": "openregs", "table": "documents", "rows": [["FDA-2011-D-0476-0009", "FDA", "FDA-2011-D-0476", "Guidance for Industry and Staff; Availability: Enforcement Policy for Premarket Notification Requirements for Certain In Vitro Diagnostic and Radiology Devices", "Notice", "Notice of Availability", "2011-12-20T05:00:00Z", 2011, 12, "2011-12-20T05:00:00Z", null, "2012-03-24T19:36:40Z", "2011-32437", 0, 0, "0900006480f86544"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2011-D-0476-0009"], "units": {}, "query_ms": 44.995133008342236, "source": "Federal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"}