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withdrawn,object_id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-0399-0002,FDA,FDA-2018-N-0399,"Medical Devices; Hematology and Pathology Devices; Classification of
Lynch Syndrome Test Systems; Correction",Rule,Correction,2018-03-14T04:00:00Z,2018,3,2018-03-14T04:00:00Z,,2018-03-14T13:48:23Z,2018-05115,0,0,090000648300e55e
FDA-2018-N-0399-0001,FDA,FDA-2018-N-0399,"Medical Devices; Hematology and Pathology Devices; Classification 
of Lynch Syndrome Test Systems",Rule,Final Rule,2018-02-27T05:00:00Z,2018,2,2018-02-27T05:00:00Z,,2018-02-27T20:03:18Z,2018-03924,0,0,0900006482f67e04