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 
 4 
 5 
 6 
 7 
 8 
 9 
 > 
 
84 records meeting your search criteria returned- Product Code: JIL Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK STATUS+ 10/28/2019
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK ADVANTUS 10/21/2019
ROCHE DIAGNOSTICS COBAS U 601 URINE ANALYZER 04/25/2019
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK STATUS+ 04/02/2019
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK STATUS+ 03/12/2019
ROCHE DIAGNOSTICS COBAS U 601 URINE ANALYZER 01/25/2019
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK STATUS+ 12/14/2018
SIEMENS HEALTHCARE DIAGNOSTICS CLINITEK STATUS+ 12/05/2018
ROCHE DIAGNOSTICS CHEMSTRIP ® 10 MD 05/07/2018
ROCHE DIAGNOSTICS CHEMSTRIP ® 10 MD 05/07/2018
-
-