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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
95 records meeting your search criteria returned- Product Code: CFR 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 INC. DIMENSION VISTA 1500 06/12/2017
ROCHE DIAGNOSTICS COBAS INTEGRA 400 PLUS 06/05/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION VISTA 1500 06/02/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. ADVIA 1800 05/31/2017
ABBOTT MANUFACTURING INC CLINICAL CHEMISTRY GLUCOSE 05/29/2017
SIEMENS HEALTHCARE DIAGNOSTICS DIMENSION VISTA 500 05/26/2017
ABBOTT MANUFACTURING INC CLINICAL CHEMISTRY GLUCOSE 05/19/2017
ROCHE DIAGNOSTICS GLUC3 GLUCOSE HK GEN.3 05/18/2017
ABBOTT MANUFACTURING INC CLINICAL CHEMISTRY GLUCOSE 05/10/2017
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION VISTA1500 04/26/2017
-
-