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withdrawn,object_id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-0061-0002,FDA,FDA-1978-N-0061,Hematology and Pathology Devices Classification of Sickle Cell Tests,Rule,Final Rule,2012-07-26T04:00:00Z,2012,7,2012-07-26T04:00:00Z,1980-10-15T03:59:59Z,2012-07-27T14:33:00Z,,0,0,09000064805622f0
FDA-1978-N-0061-0003,FDA,FDA-1978-N-0061,Accession No. 88-86-05 Box 11 - Retired,Other,Retired (RET),2012-07-26T04:00:00Z,2012,7,2012-07-26T04:00:00Z,,2012-07-26T15:40:57Z,,0,0,09000064805622f2
FDA-1978-N-0061-0004,FDA,FDA-1978-N-0061,Reference Hematology and Pathology Devices Classification of Sickle Cell Tests - Background,Supporting & Related Material,Background Material,2012-07-26T04:00:00Z,2012,7,,,2012-07-27T15:14:03Z,,0,0,090000648105e5aa
FDA-1978-N-0061-0001,FDA,FDA-1978-N-0061,"Medical Devices, Classification of Sickle Cell Tests",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2012-06-26T04:00:00Z,2012,6,2012-06-26T04:00:00Z,1979-11-14T04:59:59Z,2012-07-03T23:00:56Z,,0,0,09000064805622e7