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withdrawn,object_id
FDA-2009-N-0114-0009,FDA,FDA-2009-N-0114,Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Electronic Submission of Medical Device Registration and Listing,Notice,Notice of Approval,2013-04-19T04:00:00Z,2013,4,2013-04-19T04:00:00Z,,2013-04-19T14:24:39Z,2013-09182,0,0,090000648129c055
FDA-2009-N-0114-0008,FDA,FDA-2009-N-0114,"Implementation of Device Registration and Listing Requirements Enacted in the Public Health Security and Bioterrorism Preparedness and Response Act of 2002, the Medical Device User Fee and Modernization Act of 2002, and Title II of the Food and Drug Administration Amendments Act of 2007",Rule,Final Rule,2012-08-02T04:00:00Z,2012,8,,,2012-08-02T14:34:56Z,2012-18764,0,0,09000064810beded
FDA-2009-N-0114-0003,FDA,FDA-2009-N-0114,"Tab A - ""Draft Regulatory Action , May 5, 2010"" - [OMB Review, EO12866, RPMS Note to the DDM, 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] re FDA-2009-N-0114-0002",Supporting & Related Material,REF-Reference (internal unless indicated),2010-05-18T04:00:00Z,2010,5,,,2011-06-11T16:28:04Z,,0,0,0900006480ae7fb9
FDA-2009-N-0114-0004,FDA,FDA-2009-N-0114,"Tab B - ""Changes in the Regulatory Action - [OMB Review, EO12866, RPMS Note to the DDM, 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] re FDA-2009-N-0114-0002",Supporting & Related Material,REF-Reference (internal unless indicated),2010-05-18T04:00:00Z,2010,5,,,2011-06-11T16:28:03Z,,0,0,0900006480ae7fbc
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,,2013-07-27T23:18:10Z,,0,0,0900006480ae7f91
FDA-2009-N-0114-0001,FDA,FDA-2009-N-0114,"Implementation of Device Registration and Listing Requirements Enacted in the Public Health Security and Bioterrorism Preparedness and  Response Act of 2002, the Medical Device User Fee and Modernization Act  of 2002, and Title II of the Food and Drug Administration Amendments Act of 2007",Proposed Rule,NPR-Notice of Proposed Rule-Making,2010-03-26T04:00:00Z,2010,3,,,2011-06-11T16:28:04Z,2010-06662,0,0,0900006480ac93c0