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withdrawn,object_id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-1927-0003,FDA,FDA-1978-N-1927,Classification of Artifical Embolization Devices,Rule,Final Rule,2012-08-22T04:00:00Z,2012,8,2012-08-22T04:00:00Z,,2012-08-22T18:09:59Z,,0,0,090000648059e68e
FDA-1978-N-1927-0002,FDA,FDA-1978-N-1927,Classification of Artificial Embolization Devices - Reference,Supporting & Related Material,Reference (internal unless indicated),2012-08-22T04:00:00Z,2012,8,,,2012-08-22T18:41:07Z,,0,0,09000064810ea85e
FDA-1978-N-1927-0001,FDA,FDA-1978-N-1927,Classification of Artifical Embolization Devices,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2012-08-22T04:00:00Z,2012,8,2012-08-22T04:00:00Z,1979-01-30T04:59:59Z,2012-08-22T18:05:08Z,,0,0,090000648059e68d
FDA-1978-N-1927-0004,FDA,FDA-1978-N-1927,"Accession No. 88-86-04, Box 2 - Retired",Other,Retired (RET),2012-08-22T04:00:00Z,2012,8,2012-08-22T04:00:00Z,,2012-08-22T18:10:00Z,,0,0,090000648059e68f