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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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9 records meeting your search criteria returned- Product Code: DRM Product Problem: Therapeutic or Diagnostic Output Failure Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
PHYSIO-CONTROL LUCAS 2 08/12/2023
JOLIFE AB LUCAS 01/18/2023
STRYKER CORP / JOLIFE AB STRYKER LUCAS II AUTOMATED COMPRESSION D 05/09/2022
MICHIGAN INSTRUMENTS, LLC THUMPER 10/26/2021
MICHIGAN INSTRUMENTS, LLC THUMPER 10/06/2021
JOLIFE AB LUCAS 10/23/2020
MICHIGAN INSTRUMENTS, LLC LIFE-STAT 09/17/2019
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 07/29/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 07/17/2015
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