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withdrawn,object_id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-0611-0018,FDA,FDA-2008-D-0611,Submission and Review of Sterility Information in Premarket Notification (510(k)) Submissions for Devices Labeled as Sterile; Guidance for Industry and Food and Drug Administration Staff,Other,Guidance,2024-01-08T05:00:00Z,2024,1,2024-01-08T05:00:00Z,,2024-11-12T06:24:08Z,,1,0,0900006486384f52