{"database": "openregs", "table": "dockets", "rows": [["FDA-2000-M-0121", "FDA", "PMA Carpentier-Edwards PERIMOUNT Pericardial Bioprosthesis", "Nonrulemaking", "2021-09-01T02:01:19Z", "0b000064804cf2c3"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2000-M-0121"], "units": {}, "query_ms": 0.45862095430493355, "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"}