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withdrawn,object_id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-2017-N-5870-0001,FDA,FDA-2017-N-5870,Medical Devices; Immunology and Microbiology Devices; Classification of the Aquaporin-4 Autoantibody Immunological Test System,Rule,Final Rule,2017-10-30T04:00:00Z,2017,10,2017-10-30T04:00:00Z,,2017-10-30T17:16:31Z,2017-23489,0,0,0900006482c21ea6