• 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 
 > 
 
18 records meeting your search criteria returned- Product Code: JAA Product Problem: Degraded Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GE OEC MEDICAL SYSTEMS (SLC) 9900 12/03/2014
GE OEC MEDICAL SYSTEMS (SLC) 9800 10/15/2014
GE OEC MEDICAL SYSTEMS (SLC) 6800 08/19/2014
GE OEC MEDICAL SYSTEMS (SLC) 9900 07/11/2014
GE OEC MEDICAL SYSTEMS (SLC) 9800 05/29/2014
GE OEC MEDICAL SYSTEMS (SLC) 9800 05/21/2014
GE OEC MEDICAL SYSTEMS 9800 04/22/2014
GE OEC MEDICAL SYSTEMS GMBH 7900 04/22/2014
GE OEC MEDICAL SYSTEMS (SLC) 8800 04/14/2014
GE OEC MEDICAL SYSTEMS GMBH 7900 04/14/2014
-
-