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withdrawn,object_id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-2015-N-3838-0002,FDA,FDA-2015-N-3838,"Reference 1 - DEN100013de novo request per 513(f)(2) from Vioguard, dated November 2, 2010 re Medical Devices; General Hospital and Personal Use Devices; Classification of the Ultraviolet Radiation Chamber Disinfection Device",Supporting & Related Material,Background Material,2015-11-20T05:00:00Z,2015,11,,,2015-11-20T14:35:08Z,,0,0,0900006481d5b92c
FDA-2015-N-3838-0001,FDA,FDA-2015-N-3838,Medical Devices; General Hospital and Personal Use Devices; Classification of the Ultraviolet Radiation Chamber Disinfection Device,Rule,Final Rule,2015-11-20T05:00:00Z,2015,11,2015-11-20T05:00:00Z,,2015-11-20T14:32:07Z,2015-29660,0,0,0900006481d5e06b