• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 
 
70 records meeting your search criteria returned- Product Code: NIG Report Date From: 1/1/2016 Report Date To: 12/31/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ROCHE DIAGNOSTICS ELECSYS CA 19-9 03/10/2016
ABBOTT LABORATORIES ARCHITECT CA 19-9XR 03/10/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CA 19-9 ASSAY 02/29/2016
ROCHE DIAGNOSTICS ELECSYS CA 19-9 02/24/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR CP CA 19-9 IMMUNOASSAY 02/10/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CA 19-9 ASSAY 02/06/2016
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP CA 19-9 ASSAY 02/05/2016
ABBOTT LABORATORIES ARCHITECT CA 19-9XR 01/12/2016
ABBOTT LABORATORIES ARCHITECT CA 19-9XR 01/12/2016
SIEMENS HEALTHCARE DIAGNOSTICS INC. IMMULITE 2000 BR-MA 01/08/2016
-
-