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withdrawn,object_id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-1129-0058,FDA,FDA-2017-N-1129,"Procedures for Class II Device Exemptions from Premarket Notification, Guidance for Industry and CDRH Staff",Other,Guidance,2020-05-04T04:00:00Z,2020,5,2020-05-04T04:00:00Z,,2024-11-06T23:35:53Z,,1,0,090000648452df2a