• 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 
 > 
 
90 records meeting your search criteria returned- Product Code: MTF 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
ABBOTT IRELAND ARCHITECT TOTAL PSA 09/26/2017
ROCHE DIAGNOSTICS TOTAL PSA, TOTAL (FREE + COMPLEXED) PSA 09/15/2017
ABBOTT IRELAND ARCHITECT TOTAL PSA 08/30/2017
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP PROSTATE SPECIFIC ANTIG 07/14/2017
ROCHE DIAGNOSTICS ELECSYS TOTAL PSA IMMUNOASSAY 07/07/2017
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP PROSTATE SPECIFIC ANTIG 06/08/2017
ABBOTT IRELAND ARCHITECT TOTAL PSA 04/13/2017
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XPT PSA ASSAY 04/13/2017
SIEMENS HEALTHCARE DIAGNOSTICS, INC. ADVIA CENTAUR XP PSA ASSAY 04/05/2017
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, IMMULITE 2000 PSA 02/10/2017
-
-