{"database": "openregs", "table": "documents", "rows": [["FDA-2015-D-0025-0015", "FDA", "FDA-2015-D-0025", "Medical Device Accessories\u2014Describing Accessories and Classification Pathway for New Accessory Types; Guidance for Industry and Food and Drug Administration Staff; Availability", "Notice", "Notice of Availability", "2016-12-30T05:00:00Z", 2016, 12, "2016-12-30T05:00:00Z", null, "2016-12-30T14:17:49Z", "2016-31669", 0, 0, "0900006482441379"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2015-D-0025-0015"], "units": {}, "query_ms": 0.47734903637319803, "source": "Federal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"}