{"database": "openregs", "table": "dockets", "rows": [["FDA-1978-N-0624", "FDA", "Medical Devices Classification of Prothrombin-Proconvertin Tests and Thrombotests-RETIRED", "Rulemaking", "2021-09-01T18:03:17Z", "0b0000648057895b"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-1978-N-0624"], "units": {}, "query_ms": 0.3811339847743511, "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"}