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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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23 records meeting your search criteria returned- Product Code: DRT Product Problem: Failure of Device to Self-Test Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ZOLL MEDICAL CORPORATION X SERIES 11/05/2019
ZOLL MEDICAL CORPORATION X SERIES 10/22/2019
ZOLL MEDICAL CORPORATION X SERIES 10/17/2019
ZOLL MEDICAL CORPORATION ZOLL R-SERIES 02/15/2019
ZOLL MEDICAL CORPORATION X SERIES 01/23/2019
ZOLL MEDICAL CORPORATION X SERIES 01/15/2019
ZOLL MEDICAL CORPORATION X SERIES 12/24/2018
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 11/27/2018
ZOLL MEDICAL CORPORATION X SERIES 10/03/2018
ZOLL MEDICAL CORPORATION X SERIES 05/09/2018
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