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withdrawn,object_id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-2008-N-0393-0014,FDA,FDA-2008-N-0393,"OMB Review, Executive Order 12866, Medical Device Reporting: Electronic Submission Requirements February 14, 2014– Memorandum",Other,References (internal) (REF),2014-03-12T04:00:00Z,2014,3,2014-03-12T04:00:00Z,,2014-03-12T17:26:02Z,,0,0,0900006481661a66
FDA-2008-N-0393-0013,FDA,FDA-2008-N-0393,Medical Device Reporting: Electronic Submission Requirements,Rule,Final Rule,2014-02-14T05:00:00Z,2014,2,2014-02-14T05:00:00Z,,2014-02-14T17:29:16Z,2014-03279,0,0,09000064815663fd
FDA-2008-N-0393-0011,FDA,FDA-2008-N-0393,"Questions and Answers About Electronic Medical Device Reporting;
Availability",Notice,Notice of Availability,2014-02-14T05:00:00Z,2014,2,2014-02-14T05:00:00Z,,2014-02-14T17:07:54Z,2014-03276,0,0,09000064815661b9
FDA-2008-N-0393-0012,FDA,FDA-2008-N-0393,"Questions and Answers about eMDR - Electronic Medical Device Reporting - Guidance for Industry, User Facilities and FDA Staff",Other,Guidance,2014-02-13T05:00:00Z,2014,2,2014-02-13T05:00:00Z,,2024-11-11T20:48:51Z,,1,0,090000648156798c