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withdrawn,object_id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-2017-N-6643-0001,FDA,FDA-2017-N-6643,"Medical Devices; Hematology and Pathology Devices; Classification of
the Flow Cytometric Test System for Hematopoietic Neoplasms",Rule,Final Rule,2017-12-27T05:00:00Z,2017,12,2017-12-27T05:00:00Z,,2017-12-27T17:36:02Z,2017-27855,0,0,0900006482d7617f