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withdrawn,object_id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-2017-N-6730-0035,FDA,FDA-2017-N-6730,Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals,Notice,Notice of Approval,2018-09-28T04:00:00Z,2018,9,2018-09-28T04:00:00Z,,2018-10-23T15:15:20Z,2018-21209,0,0,09000064837801da
FDA-2017-N-6730-0034,FDA,FDA-2017-N-6730,Medical Devices and Device-Led Combination Products: Voluntary Malfunction Summary Reporting Program for Manufacturers,Rule,Final Rule,2018-08-17T04:00:00Z,2018,8,2018-08-17T04:00:00Z,,2024-08-29T18:23:06Z,2018-17770,0,0,090000648363074e
FDA-2017-N-6730-0033,FDA,FDA-2017-N-6730,"Agency Information Collection Activities; Submission for Office of
Management and Budget Review; Comment Request; Voluntary
Malfunction Summary Reporting Program for Manufacturers",Notice,30 Day Proposed Information Collection,2018-06-08T04:00:00Z,2018,6,2018-06-08T04:00:00Z,2018-07-10T03:59:59Z,2018-06-10T01:03:01Z,2018-12336,0,0,0900006483398b52