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withdrawn,object_id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-2024-N-5375-0001,FDA,FDA-2024-N-5375,"Revocation of Authorization of Emergency Use of B. Braun Medical’s Perfusor Space Syringe Infusion Pump System, Infusomat Space Volumetric Infusion Pump System, and Outlook ES; Availability",Notice,Announcement,2024-12-12T05:00:00Z,2024,12,,,2024-12-13T16:07:35Z,2024-29247,0,0,090000648686642c