{"database": "openregs", "table": "documents", "rows": [["FDA-2014-N-1210-0002", "FDA", "FDA-2014-N-1210", "List of References for Reclassification of Electroconvulsive Therapy (ECT) Devices Intended for Use in Treating Severe Major Depressive Episode in Patients 18 Years of Age and Older Who are Treatment Resistant or Require a Rapid Response; Effective Date of Requirement for Premarket Approval for ECT Devices for Certain Specified Intended Uses Proposed Order", "Supporting & Related Material", "List", "2015-12-29T05:00:00Z", 2015, 12, null, null, "2015-12-29T17:24:43Z", null, 0, 0, "0900006481dd8bf5"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2014-N-1210-0002"], "units": {}, "query_ms": 65.25655603036284, "source": "Federal Register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"}