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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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11 records meeting your search criteria returned- Product Code: DRO Product Problem: Output Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 12/30/2019
ZOLL MEDICAL CORPORATION M SERIES 12/16/2019
ZOLL MEDICAL CORPORATION M SERIES 08/28/2019
ZOLL MEDICAL CORPORATION M SERIES 07/30/2019
ZOLL MEDICAL CORPORATION M SERIES 05/30/2019
ZOLL MEDICAL CORPORATION M SERIES 02/14/2019
ZOLL MEDICAL CORPORATION M SERIES 08/02/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 01/19/2016
ZOLL MEDICAL CORPORATION M SERIES 12/29/2015
ZOLL MEDICAL CORPORATION M SERIES 11/24/2015
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