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withdrawn,object_id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-1978-N-0630-0003,FDA,FDA-1978-N-0630,"Reference List and Reference 1 - ""Transcript of the Hematology Device Classification Panel Meeting, June 14, 1977 - Background",Supporting & Related Material,BKG-Background Material,2008-10-01T04:00:00Z,2008,10,,,2008-10-02T00:27:22Z,,0,0,0900006480578f4c
FDA-1978-N-0630-0002,FDA,FDA-1978-N-0630,Hematology and Pathology Devices Classification of Automated Heparin Analyzers,Rule,NFR-Notice of Final Rule,2008-10-01T04:00:00Z,2008,10,2008-10-01T04:00:00Z,1980-10-15T03:59:59Z,2008-10-02T00:26:56Z,,0,0,0900006480578f48
FDA-1978-N-0630-0001,FDA,FDA-1978-N-0630,Devices Classification of Automated Heparin Analyzers,Proposed Rule,NPR-Notice of Proposed Rule-Making,2008-10-01T04:00:00Z,2008,10,2008-10-01T04:00:00Z,1979-11-14T04:59:59Z,2008-10-02T00:26:54Z,,0,0,0900006480578f42