{"database": "openregs", "table": "documents", "rows": [["FDA-2011-D-0790-0035", "FDA", "FDA-2011-D-0790", "Food and Drug Administration Decisions for Investigational Device\nExemption Clinical Investigations: Guidance for Sponsors, Clinical\nInvestigators, Institutional Review Boards, and Food and Drug\nAdministration Staff; Availability", "Notice", "Notice of Availability", "2014-08-19T04:00:00Z", 2014, 8, "2014-08-19T04:00:00Z", null, "2014-08-19T14:35:26Z", "2014-19577", 0, 0, "090000648182f7fb"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2011-D-0790-0035"], "units": {}, "query_ms": 0.4739239811897278, "source": "Federal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"}