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withdrawn,object_id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-2018-D-4115-0001,FDA,FDA-2018-D-4115,"Clarification of Radiation Control Regulations for Manufacturers of
Diagnostic X-Ray Equipment; Draft Guidance for Industry and Food and
Drug Administration Staff; Availability",Notice,Notice of Availability,2018-12-17T05:00:00Z,2018,12,2018-12-17T05:00:00Z,2019-02-16T04:59:59Z,2024-11-12T22:52:39Z,2018-27236,1,0,090000648399cd0c
FDA-2018-D-4115-0002,FDA,FDA-2018-D-4115,Draft Guidance for Industry and FDA_Clarification of Radiation Control Regulations for Diagnostic X-Ray Equipment_issued December 17 2018,Other,Guidance,2018-12-17T05:00:00Z,2018,12,2018-12-17T05:00:00Z,2019-02-16T04:59:59Z,2024-09-30T21:03:13Z,,0,0,090000648399d6ea