• 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 
 > 
 
41 records meeting your search criteria returned- Product Code: KQO Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS URISYS 1100 03/07/2024
ROCHE DIAGNOSTICS COBAS U 411 URINE ANALYZER 02/16/2024
ACON LABORATORIES, INC. MCKESSON CONSULT 120 URINE ANALYZER 01/19/2024
SIEMENS HEALTHCARE DIAGNOSTICS INC. CLINITEK ADVANTUS 01/10/2024
ROCHE DIAGNOSTICS COBAS U 411 URINE ANALYZER 12/21/2023
ACON LABORATORIES, INC. PRO ADVANTAGE URINE ANALYZER 12/21/2023
ACON LABORATORIES, INC. MCKESSON CONSULT U120 URINE ANALYZER 10/24/2023
ACON LABORATORIES, INC. MEDLINE 120 MINI URINE ANALYZER 09/22/2023
BECKMAN COULTER IRIS LABORATORY INSTRUMENT 08/12/2023
ROCHE DIAGNOSTICS COBAS U 411 URINE ANALYZER 08/09/2023
-
-