documents: FDA-2024-N-5375-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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

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