{"database": "openregs", "table": "documents", "rows": [["FDA-2009-N-0114-0002", "FDA", "FDA-2009-N-0114", "OMB Review, EO12866, Regulatory Policy and Management Staff Note to the Division of Dockets Management, May 5, 2010 - [Implementation of Device Registration and Listing Requirements Enacted in Section 321 of the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, and Title II of the FDAAA 2007; Proposed Rule, March 26, 2010] - Reference", "Other", "REF-Reference", "2010-05-18T04:00:00Z", 2010, 5, "2010-05-18T04:00:00Z", null, "2013-07-27T23:18:10Z", null, 0, 0, "0900006480ae7f91"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2009-N-0114-0002"], "units": {}, "query_ms": 20.41618386283517, "source": "Federal Register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"}