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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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82 records meeting your search criteria returned- Product Code: DRT Product Problem: Device Displays Incorrect Message Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
WELCH ALLYN PROPAQ CS 246 07/28/2016
PHILIPS MEDICAL SYSTEMS V24/26 COMPONENT MONITORING SYSTEM 05/25/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 05/24/2016
ZOLL MEDICAL CORPORATION X SERIES 02/08/2016
ZOLL MEDICAL CORPORATION X SERIES 12/31/2015
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 12/17/2015
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 09/30/2015
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 09/28/2015
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 09/04/2015
WELCH ALLYN PROPAQ ENCORE 04/17/2015
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