{"database": "openregs", "table": "documents", "rows": [["FDA-2017-N-6356-0001", "FDA", "FDA-2017-N-6356", "Investigational In Vitro Diagnostics Used in Clinical Investigations of\nTherapeutic Products; Draft Guidance for Industry, Food and Drug\nAdministration Staff, Sponsors, and Institutional Review Boards;  Availability", "Notice", "Notice of Availability", "2017-12-18T05:00:00Z", 2017, 12, "2017-12-18T05:00:00Z", "2018-03-20T03:59:59Z", "2018-03-20T13:01:12Z", "2017-27155", 0, 0, "0900006482d30343"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2017-N-6356-0001"], "units": {}, "query_ms": 5.280532990582287, "source": "Federal Register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"}