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withdrawn,object_id
FDA-2008-D-0611-0001,FDA,FDA-2008-D-0611,Draft Guidance for Industry and Food and Drug Administration Staff; Submission and Review of Sterility Information in Premarket Notification Submissions for Devices Labeled as Sterile; Availability,Notice,NAD-Notice of Availability of Data,2008-12-12T05:00:00Z,2008,12,2008-12-12T05:00:00Z,2009-03-13T03:59:59Z,2009-03-19T21:37:24Z,E8-29413,0,0,09000064807d8787
FDA-2008-D-0611-0002,FDA,FDA-2008-D-0611,Draft Guidance for Industry and FDA Staff - Submission and review of sterility information in premarket notification (510(k)) submissions for devices labeled as sterile - Guidance,Other,GDL-Guidance (Supporting and Related Materials),2008-12-12T05:00:00Z,2008,12,,,2013-07-27T22:33:12Z,,0,0,09000064807d88e6