{"database": "openregs", "table": "dockets", "rows": [["FDA-2004-D-0247", "FDA", "Guidance for Industry and Food and Drug Administration; Class II Special Controls Guidance Document: Implantable Radiofrequency Transponder System for Patient Identification and Health Information", "Nonrulemaking", "2021-09-01T01:02:15Z", "0b00006480471af2"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2004-D-0247"], "units": {}, "query_ms": 0.4618550883606076, "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"}