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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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16 records meeting your search criteria returned- Product Code: DRT Product Problem: Misassembly by Users Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION ZM-531PA 08/20/2018
NIHON KOHDEN CORPORATION ZM-521PA 08/17/2018
NIHON KOHDEN CORPORATION ZM-531PA 06/12/2018
NIHON KOHDEN CORPORATION ZM-530PA 05/03/2018
NIHON KOHDEN CORPORATION ZM-521PA 04/27/2018
NIHON KOHDEN CORPORATION ZM-520PA 04/20/2018
NIHON KOHDEN CORPORATION ZM-521PA 04/20/2018
NIHON KOHDEN CORPORATION ZM-521PA 04/18/2018
NIHON KOHDEN CORPORATION ZM-521PA 04/18/2018
NIHON KOHDEN CORPORATION ZM-521PA 04/18/2018
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