{"database": "openregs", "table": "documents", "rows": [["FDA-2003-N-0395-0002", "FDA", "FDA-2003-N-0395", "Agency Information Collection Activities; Submission for OMB Review; Comment Request; Export of Medical Devices-Foreign Letters of Approval", "Notice", "30 Day Proposed Information Collection", "2003-08-27T04:00:00Z", 2003, 8, "2003-08-25T04:00:00Z", "2003-09-25T03:59:59Z", "2025-03-04T15:11:28Z", "03-21625", 0, 0, "09000064804a194c"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2003-N-0395-0002"], "units": {}, "query_ms": 0.3954259445890784, "source": "Federal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"}