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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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154 records meeting your search criteria returned- Product Code: DRO Patient Problem: No Patient Involvement Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 08/04/2016
ZOLL MEDICAL CORPORATION M SERIES 08/02/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 07/01/2016
ZOLL MEDICAL CORPORATION M SERIES 06/13/2016
ZOLL MEDICAL CORPORATION E SERIES DEFIBRILLATOR 05/18/2016
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 03/31/2016
ZOLL MEDICAL CORPORATION X SERIES 03/22/2016
ZOLL MEDICAL CORPORATION X SERIES 03/21/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 03/07/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 03/04/2016
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