{"database": "openregs", "table": "documents", "rows": [["FDA-2016-N-1593-0003", "FDA", "FDA-2016-N-1593", "Agency Information Collection Activities; Proposed Collection;\nComment Request; Medical Device Accessories", "Notice", "60 Day Proposed Information Collection", "2019-04-04T04:00:00Z", 2019, 4, "2019-04-04T04:00:00Z", "2019-06-04T03:59:59Z", "2019-04-04T13:42:58Z", "2019-06551", 0, 0, "0900006483b63134"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2016-N-1593-0003"], "units": {}, "query_ms": 7.621805008966476, "source": "Federal Register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"}