{"database": "openregs", "table": "documents", "rows": [["FDA-2018-N-4206-0006", "FDA", "FDA-2018-N-4206", "Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Medical Device User Fee Small Business Qualification and Certification", "Notice", "30 Day Proposed Information Collection", "2022-04-25T04:00:00Z", 2022, 4, "2022-04-25T04:00:00Z", "2022-05-26T03:59:59Z", "2022-04-25T12:35:34Z", "2022-08726", 0, 0, "0900006485031c96"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2018-N-4206-0006"], "units": {}, "query_ms": 0.9352581109851599, "source": "Federal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"}