{"database": "openregs", "table": "documents", "rows": [["FDA-2013-N-0370-0009", "FDA", "FDA-2013-N-0370", "Agency Information Collection Activities; Proposed Collection; Comment Request; Export of Medical\nDevices; Foreign Letters of Approval", "Notice", "60 Day Proposed Information Collection", "2022-01-28T05:00:00Z", 2022, 1, "2022-01-28T05:00:00Z", "2022-03-30T03:59:59Z", "2022-10-28T19:29:43Z", "2022-01793", 0, 0, "0900006484f410f6"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2013-N-0370-0009"], "units": {}, "query_ms": 111.87785502988845, "source": "Federal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"}