• 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
 

 
 
6 records meeting your search criteria returned- Product Code: KHE Product Problem: Incorrect, Inadequate or Imprecise Result or Readings Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BECKMAN COULTER, INC. HEMOCCULT 01/28/2021
BECKMAN COULTER, INC. 66040 GASTROCCULT TEST FOR GASTRIC OCCUL 08/16/2019
ROCHE DIAGNOSTICS URISYS 1100 08/26/2014
ROCHE DIAGNOSTICS URISYS 1100 08/26/2014
ROCHE DIAGNOSTICS URISYS 1100 06/24/2014
ROCHE DIAGNOSTICS URISYS 1100 03/27/2014
-
-