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 
 
 
41 records meeting your search criteria returned- Product Code: JAK Product Problem: Device Inoperable Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NEUROLOGICA CORPORATION CERETOM NL3000 08/09/2016
NEUROLOGICA CORPORATION CERETOM NL3000 07/19/2016
COVIDIEN, INC. SUPERDIMENSION NAVIGATION SYSTEM 03/21/2016
PHILIPS MEDICAL SYSTEMS BRILLANCE 02/10/2016
PHILLIPS MEDICAL SYSTEMS INC PHILLIPS ICT 11/04/2015
TOSHIBA AMERICA MEDICAL SYSTEM, INC. SYSTEM, X-RAY, TOMOGRAPHY, COMPUTED 10/16/2015
TOSHIBA TOSHIBA CAT SCAN MACHINE 09/28/2015
SIEMENS HEALTHCARE GMBH SOMATOM SENSATION 64 06/05/2015
PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC BRILLIANCE 10 AIR 05/12/2015
GE MEDICAL SYSTEMS INFORMATION TECH. unknown brand name 09/26/2014
-
-