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withdrawn,object_id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-1501-0006,FDA,FDA-1978-N-1501,Cross Reference Sheet - Background Material,Supporting & Related Material,Background Material,2012-08-14T04:00:00Z,2012,8,,,2012-08-14T14:34:58Z,,0,0,09000064810d44ff
FDA-1978-N-1501-0002,FDA,FDA-1978-N-1501,Proposed Rules for Device Classification - Notice of Withdrawal,Notice,Withdrawal,2012-07-13T04:00:00Z,2012,7,2012-07-13T04:00:00Z,,2012-08-14T14:23:34Z,,0,0,090000648059b840
FDA-1978-N-1501-0004,FDA,FDA-1978-N-1501,"Accession No. 88-86-09, Box 4 - Retired",Other,Retired (RET),2012-07-13T04:00:00Z,2012,7,2012-07-13T04:00:00Z,,2012-08-14T14:29:35Z,,0,0,090000648059b842
FDA-1978-N-1501-0003,FDA,FDA-1978-N-1501,Transfer of Administrative Record for Cirumcision Instrument - Memorandum,Other,Memorandum,2012-07-13T04:00:00Z,2012,7,2012-07-13T04:00:00Z,,2012-08-14T14:25:58Z,,0,0,090000648059b841
FDA-1978-N-1501-0001,FDA,FDA-1978-N-1501,Classification of Circumcision Instruments - Notice of Proposed Rule,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2012-07-13T04:00:00Z,2012,7,2012-07-13T04:00:00Z,1981-03-25T04:59:59Z,2012-07-13T12:35:12Z,,0,0,090000648059b83e