{"database": "openregs", "table": "documents", "rows": [["FDA-2021-N-0998-0001", "FDA", "FDA-2021-N-0998", "Medical Devices; General Hospital and Personal Use Devices; Classification of the Alternate Controller Enabled Infusion Pump", "Rule", "Final Rule", "2022-02-04T05:00:00Z", 2022, 2, "2022-02-04T05:00:00Z", null, "2022-02-04T17:19:53Z", "2022-02369", 0, 0, "0900006484f54a4f"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2021-N-0998-0001"], "units": {}, "query_ms": 55.147493025287986, "source": "Federal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"}