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withdrawn,object_id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-2018-N-3634-0001,FDA,FDA-2018-N-3634,"Medical Devices; Ophthalmic Devices; Classification of the Intranasal
Electrostimulation Device for Dry Eye Symptoms",Rule,Final Rule,2018-10-19T04:00:00Z,2018,10,2018-10-19T04:00:00Z,,2018-10-19T13:15:29Z,2018-22785,0,0,090000648380aad9