{"database": "openregs", "table": "documents", "rows": [["FDA-2012-N-1021-0033", "FDA", "FDA-2012-N-1021", "Medical Device User Fee and Modernization Act; Notice to Public of\nWeb Site Location of Fiscal Year 2017 Proposed Guidance Development", "Notice", "Announcement", "2016-12-23T05:00:00Z", 2016, 12, "2016-12-23T05:00:00Z", "2017-02-22T04:59:59Z", "2019-10-15T14:26:03Z", "2016-31006", 0, 0, "0900006482433eae"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2012-N-1021-0033"], "units": {}, "query_ms": 45.93004897469655, "source": "Federal Register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"}