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

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
 

 
 
7 records meeting your search criteria returned- Product Code: KHO Product Problem: Use of Device Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TOSOH HI-TEC, INC. AIA-900 12/11/2022
ORTHO-CLINICAL DIAGNOSTICS VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 05/05/2021
TOSOH CORPORATION AIA-900 06/02/2020
TOSOH CORPORATION AIA-360 06/20/2019
TOSOH CORPORATION AIA-360 05/30/2019
TOSOH CORPORATION AIA-2000 05/02/2019
TOSOH CORPORATION AIA-2000 05/02/2019
-
-