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withdrawn,object_id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-D-0386-0010,FDA,FDA-2009-D-0386,"Guidance for Industry and Staff; Establishing Performance Characteristics of In Vitro Diagnostic Devices for the Detection, etc., of Human Papillomaviruses",Other,Guidance,2011-11-28T05:00:00Z,2011,11,2011-11-28T05:00:00Z,,2015-07-29T16:44:57Z,,0,0,0900006480f7483f
FDA-2009-D-0386-0009,FDA,FDA-2009-D-0386,"Guidance for Industry and Staff; Availability: Establishing Performance Characteristics of In Vitro Diagnostic Devices for the Detection, etc., of Human Papillomaviruses",Notice,Notice of Availability,2011-11-28T05:00:00Z,2011,11,2011-11-28T05:00:00Z,,2015-07-29T16:44:35Z,2011-30552,0,0,0900006480f743be