• 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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
115 records meeting your search criteria returned- Product Code: KHO Product Problem: High Test Results Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TOSOH HI-TEC, INC. AIA-900 07/30/2024
TOSOH HI-TEC, INC. AIA-2000 ST 05/06/2024
ORTHO-CLINICAL DIAGNOSTICS, INC. VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 12/21/2023
ORTHO-CLINICAL DIAGNOSTICS, INC. VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 10/26/2023
ORTHO-CLINICAL DIAGNOSTICS, INC. VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 08/29/2023
TOSOH HI-TEC, INC. AIA-2000 03/23/2023
ORTHO-CLINICAL DIAGNOSTICS, INC. VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 03/06/2023
TOSOH HI-TEC, INC. AIA-900 02/20/2023
ORTHO-CLINICAL DIAGNOSTICS VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM 03/31/2022
ORTHO-CLINICAL DIAGNOSTICS VITROS ECI IMMUNODIAGNOSTIC SYSTEM 11/22/2021
-
-