{"database": "openregs", "table": "dockets", "rows": [["FDA-2026-N-3946", "FDA", "Medical Devices; Cardiovascular Devices; Classification of the Laser-Powered Inferior Vena Cava Filter Retrieval Catheter", "Rulemaking", "2026-04-30T13:22:35Z", "0b000064b9267937"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2026-N-3946"], "units": {}, "query_ms": 0.4268930060788989, "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"}