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withdrawn,object_id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-2006-N-0178-0002,FDA,FDA-2006-N-0178,Reference,Supporting & Related Material,REF-Reference (internal unless indicated),2006-10-31T05:00:00Z,2006,10,,,2008-04-11T23:10:00Z,,0,0,0900006480450b94
FDA-2006-N-0178-0004,FDA,FDA-2006-N-0178,Reference,Supporting & Related Material,REF-Reference (internal unless indicated),2006-10-31T05:00:00Z,2006,10,,,2008-04-11T23:10:00Z,,0,0,0900006480450b9c
FDA-2006-N-0178-0001,FDA,FDA-2006-N-0178,General and Plastic Surgery Devices; Reclassification of the Absorbable Hemostatic Device,Proposed Rule,NPR-Notice of Proposed Rule-Making,2006-10-31T05:00:00Z,2006,10,2006-10-30T05:00:00Z,2007-01-30T04:59:59Z,2008-07-07T18:20:13Z,,0,0,0900006480450b90
FDA-2006-N-0178-0003,FDA,FDA-2006-N-0178,Reference,Supporting & Related Material,REF-Reference (internal unless indicated),2006-10-31T05:00:00Z,2006,10,,,2008-04-11T23:10:00Z,,0,0,0900006480450b9b