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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS HEALTHCARE / PHILIPS ELECTRONICS COMBI DIAGNOST R90 FLUROSCOPY ROOM SITE 06/10/2022
GE OEC MEDICAL SYSTEMS (SLC) 9900 04/16/2015
GE OEC MEDICAL SYSTEMS (SLC) 9800 04/15/2015
GE OEC MEDICAL SYSTEMS (SLC) 9800 04/14/2015
GE OEC MEDICAL SYSTEMS (SLC) 9800 04/02/2015
GE OEC MEDICAL SYSTEMS (SLC) 9900 03/11/2015
GE OEC MEDICAL SYSTEMS (SLC) 6600 03/04/2015
GE OEC MEDICAL SYSTEMS (SLC) 8800 03/04/2015
GE OEC MEDICAL SYSTEMS 9900 03/04/2015
GE OEC MEDICAL SYSTEMS 9900 03/04/2015
-
-