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
 

 
 
 1 
 2 
 3 
 > 
 
30 records meeting your search criteria returned- Product Code: KQO Product Problem: False Positive Result Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS URISYS 1100 10/28/2020
ROCHE DIAGNOSTICS URISYS 1100 07/28/2020
ROCHE DIAGNOSTICS COBAS U411 TEST SYSTEM 05/05/2020
ROCHE DIAGNOSTICS URISYS 1100 04/24/2020
ROCHE DIAGNOSTICS COBAS U411 TEST SYSTEM 01/23/2020
ROCHE DIAGNOSTICS URISYS 1100 01/21/2020
ROCHE DIAGNOSTICS URISYS 1100 12/06/2019
ROCHE DIAGNOSTICS URISYS 1100 12/03/2019
ROCHE DIAGNOSTICS COBAS U411 TEST SYSTEM 12/03/2019
ROCHE DIAGNOSTICS URISYS 1100 10/28/2019
-
-