• 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 
 10 
 > 
 
123 records meeting your search criteria returned- Product Code: IZI Report Date From: 1/1/2014 Report Date To: 12/31/2014

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GE MEDICAL SYSTEMS SCS INNOVA IGS 540 12/26/2014
PHILIPS HEALTHCARE ALLURA XPER FD10 12/22/2014
PHILIPS HEALTHCARE ALLURA XPER FD10 12/18/2014
PHILIPS HEALTHCARE ALLURA XPER FD20 12/17/2014
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD20 OR TABLE 12/17/2014
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD10 12/17/2014
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD20 12/17/2014
PHILLIPS, NEDERLAND B.V. PHILLIPS 12/11/2014
PHILIPS HEALTHCARE OMNIDIAGNOST ELEVA 12/04/2014
PHILIPS HEALTHCARE ALLURA XPER FD10 C 12/03/2014
-
-