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withdrawn,object_id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-0114-0008,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