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withdrawn,object_id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-1992-S-0039-0060,FDA,FDA-1992-S-0039,"FDA/CDRH Memo to the Division of Dockets Management Submission of Device Information (DI) record to the Global Unique Device Identification Database (GUDID), in compliance with the Unique Device Identification Rule - Memorandum",Supporting & Related Material,Background Material,2013-12-02T05:00:00Z,2013,12,,,2013-12-02T21:29:02Z,,0,0,09000064814a18df