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withdrawn,object_id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-2014-M-1957-0001,FDA,FDA-2014-M-1957,"Medical Devices; Obstetrical and Gynecological Devices; Classification
of the Assisted Reproduction Embryo Image Assessment System",Rule,Final Rule,2015-02-26T05:00:00Z,2015,2,2015-02-26T05:00:00Z,,2015-02-26T15:14:46Z,2015-03934,0,0,0900006481a1907d
FDA-2014-M-1957-0002,FDA,FDA-2014-M-1957,"Reference 1 K120427 De Novo Request from Auxogyn, Inc, dated August 23, 2012 re Medical Devices; Obstetrical and Gynecological Devices; Classification of the Assisted Reproduction Embryo Image Assessment System, FDA-2014-M-1957-0001",Supporting & Related Material,Background Material,2015-02-26T05:00:00Z,2015,2,,,2015-02-26T22:22:59Z,,0,0,0900006481a1b16c