{"database": "openregs", "table": "dockets", "rows": [["FDA-2026-N-5196", "FDA", "Medical Devices; Gastroenterology-Urology Devices; Classification of the Orally Ingested Transient Device for Constipation", "Rulemaking", "2026-06-01T14:27:55Z", "0b000064b92cfd24"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2026-N-5196"], "units": {}, "query_ms": 0.2245820069219917, "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"}