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withdrawn,object_id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-2016-N-1268-0001,FDA,FDA-2016-N-1268,Medical Devices: Ophthalmic Devices; Classification of the Diurnal Pattern Recorder System,Rule,Final Rule,2016-05-31T04:00:00Z,2016,5,2016-05-31T04:00:00Z,,2016-05-31T13:15:49Z,2016-12683,0,0,0900006481fff5c5