{"database": "openregs", "table": "documents", "rows": [["FDA-2015-D-3787-0009", "FDA", "FDA-2015-D-3787", "Electromagnetic Compatibility (EMC) of Medical Devices; Draft Guidance for Industry and Food and Drug Administration Staff", "Other", "Guidance", "2020-11-17T05:00:00Z", 2020, 11, "2020-11-17T05:00:00Z", "2021-02-17T04:59:59Z", "2022-06-07T12:17:12Z", null, 0, 0, "0900006484962b1e"]], "columns": ["id", "agency_id", "docket_id", "title", "document_type", "subtype", "posted_date", "posted_year", "posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2015-D-3787-0009"], "units": {}, "query_ms": 83.17491295747459, "source": "Federal Register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"}