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withdrawn,object_id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-1610-0002,FDA,FDA-2017-N-1610,"Medical Devices; Exemptions From Premarket Notification for Class I and
Class II Devices",Rule,Final Rule,2019-12-30T05:00:00Z,2019,12,2019-12-30T05:00:00Z,,2019-12-30T16:04:58Z,2019-27394,0,0,0900006484256f8e
FDA-2017-N-1610-0001,FDA,FDA-2017-N-1610,Medical Devices: Exemptions from Premarket Notification; Class I Devices,Notice,Determinations,2017-04-13T04:00:00Z,2017,4,2017-04-13T04:00:00Z,,2017-04-13T14:18:37Z,2017-07468,0,0,0900006482551ce0