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withdrawn,object_id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-0571-0001,FDA,FDA-2008-N-0571,"Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry and Food and Drug Administration Staff; Compliance With the Medical Device User Fee and Modernization Act of 2002, as Amended: Prominent and Conspicous Mark of Manufacturers on Single-Use Devices (formerly ""Reprocessed Single-Use Device Labeling"")",Notice,N-Notice,2008-11-18T05:00:00Z,2008,11,2008-11-18T05:00:00Z,2009-01-17T04:59:59Z,2024-11-12T04:25:39Z,,1,0,09000064807b0083