• 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 
 > 
 
54 records meeting your search criteria returned- Product Code: JIL 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
SIEMENS HEALTHCARE DIAGNOSTICS INC. CLINITEK STATUS+ 04/13/2023
ROCHE DIAGNOSTICS COBAS U 601 URINE ANALYZER 03/30/2023
SIEMENS HEALTHCARE DIAGNOSTICS INC. CLINITEK STATUS+ 03/28/2023
ROCHE DIAGNOSTICS CHEMSTRIP 10 MD 03/16/2023
ASCENSIA DIABETES CARE US INC. KETO-DIASTIX REAGENT STRIPS FOR URINALYS 02/24/2023
ROCHE DIAGNOSTICS CHEMSTRIP 10 MD 02/20/2023
ROCHE DIAGNOSTICS CHEMSTRIP 10 MD 12/22/2022
SIEMENS HEALTHCARE DIAGNOSTICS INC. CLINITEK STATUS+ 12/22/2022
SIEMENS HEALTHCARE DIAGNOSTICS INC. CLINITEK STATUS+ 12/08/2022
SIEMENS HEALTHCARE DIAGNOSTICS INC. CLINITEK STATUS+ 09/23/2022
-
-