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withdrawn,object_id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-0386-0005,FDA,FDA-2009-D-0386,"Enclosure - ""Lee, et al., Signature Sequence Validation of Human Papillomavirus"" - [Sin Hang Lee, MD (Milford Hospital) - Comment]",Supporting & Related Material,,2009-11-05T00:00:00Z,2009,11,,,2009-11-06T01:34:42Z,,0,1,0900006480a4f31c
FDA-2009-D-0386-0001,FDA,FDA-2009-D-0386,Draft Guidance for Industry and Food and Drug Administration Staff; Establishing the Performance Characteristics of In Vitro Diagnostic Devices for the Detection or Detection and Differentiation of Human Papillomaviruses; Availability,Notice,Notice of Availability,2009-09-09T04:00:00Z,2009,9,2009-09-09T04:00:00Z,2009-12-09T04:59:59Z,2015-07-29T16:43:45Z,E9-21725,0,0,0900006480a1f23a
FDA-2009-D-0386-0002,FDA,FDA-2009-D-0386,Establishing the Performance Characteristics of In Vitro Diagnostic Devices for the Detection or Detection and Differentiation of Human Papillomaviruses - Draft Guidance,Other,GDL-Guidance (Supporting and Related Materials),2009-09-09T04:00:00Z,2009,9,2009-09-09T04:00:00Z,,2024-11-12T04:40:42Z,,1,0,0900006480a1f52d