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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
 

 
 
9 records meeting your search criteria returned- Product Code: DRT Product Problem: Device Sensing Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION ZM-531PA 03/11/2021
NIHON KOHDEN CORPORATION ZM-531PA 03/11/2021
NIHON KOHDEN CORPORATION ZM-520PA 06/28/2018
NIHON KOHDEN CORPORATION GZ-120PA 04/17/2018
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 02/29/2016
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 01/05/2016
ZOLL MEDICAL CORPORATION X SERIES 11/18/2015
ZOLL MEDICAL CORPORATION X SERIES 11/16/2015
ZOLL MEDICAL CORPORATION R SERIES DEFIBRILLATOR 11/09/2015
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