• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 
 1 
 2 
 > 
 
15 records meeting your search criteria returned- Product Code: DRT Product Problem: Application Program Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NIHON KOHDEN CORPORATION GZ-130PA 02/05/2024
NIHON KOHDEN CORPORATION GZ-130PA 09/22/2023
NIHON KOHDEN CORPORATION GZ-130PA 05/07/2022
NIHON KOHDEN CORPORATION GZ-130PA 03/23/2022
NIHON KOHDEN CORPORATION GZ-130PA 03/16/2022
NIHON KOHDEN CORPORATION GZ-130PA 02/18/2022
NIHON KOHDEN CORPORATION GZ-130PA 02/12/2021
NIHON KOHDEN CORPORATION NI 02/12/2021
NIHON KOHDEN CORPORATION GZ-120PA 11/04/2020
NIHON KOHDEN CORPORATION GZ-120PA 08/27/2020
-
-