• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
152 records meeting your search criteria returned- Product Code: KQO Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE DIAGNOSTICS INC. CLINITEK ATLAS 07/15/2020
ROCHE DIAGNOSTICS COBAS U411 TEST SYSTEM 05/05/2020
ROCHE DIAGNOSTICS COBAS U411 TEST SYSTEM 03/04/2020
ROCHE DIAGNOSTICS COBAS U411 TEST SYSTEM 01/23/2020
ROCHE DIAGNOSTICS URISYS 1100 12/18/2019
ROCHE DIAGNOSTICS URISYS 1100 12/06/2019
ROCHE DIAGNOSTICS URISYS 1100 12/03/2019
ROCHE DIAGNOSTICS COBAS U411 TEST SYSTEM 12/03/2019
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK ATLAS 11/25/2019
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK ATLAS 11/25/2019
-
-