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withdrawn,object_id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-2013-M-0042-0002,FDA,FDA-2013-M-0042,"Medical Devices; Neurological Devices; Classification of the
Neuropsychiatric Interpretive Electroencephalograph Assessment
Aid",Rule,Final Rule,2014-02-18T05:00:00Z,2014,2,2014-02-18T05:00:00Z,,2014-02-19T19:05:29Z,2014-03388,0,0,0900006481576844
FDA-2013-M-0042-0001,FDA,FDA-2013-M-0042,Medical Devices: General Hospital and Personal Use Monitoring Devices; Classification of the Ingestible Event Marker,Rule,Final Rule,2013-05-16T04:00:00Z,2013,5,,,2013-05-16T14:06:32Z,2013-11628,0,0,09000064812e7644