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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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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93 records meeting your search criteria returned- Product Code: DRO Report Date From: 1/1/2019 Report Date To: 12/31/2019

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ManufacturerBrand NameDate Report Received
COVIDIEN UNKNOWN ELECTRODES, LEADWIRES, CABLES 06/05/2019
ZOLL MEDICAL CORPORATION M SERIES 05/30/2019
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 05/30/2019
COVIDIEN CADENCE PHYSIO QC ADULT RTS 05/29/2019
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 05/28/2019
ZOLL MEDICAL CORPORATION X SERIES 05/24/2019
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 05/23/2019
COVIDIEN ELECTRODE ADULT 4.5X6.25 DEFIBRILATION 05/20/2019
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 05/20/2019
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 05/14/2019
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