Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
  • Print
  • Share
  • E-mail
-
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
 

 
 
7 records meeting your search criteria returned- Product Code: DRT Product Problem: Image Display Error/Artifact Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION ZM-530PA 03/13/2024
NIHON KOHDEN CORPORATION ZM-530PA 03/06/2024
NIHON KOHDEN CORPORATION ZM-520PA 02/02/2024
NIHON KOHDEN CORPORATION GZ-130PA 12/14/2023
NIHON KOHDEN CORPORATION GZ-120PA 11/02/2023
STRYKER LIFEPAK 15 MONITOR / DEFIBRILLATOR 03/18/2019
NIHON KOHDEN CORPORATION ZM-530PA 04/19/2017
-
-