• 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 
 > 
 
103 records meeting your search criteria returned- Product Code: IYE Patient Problem: No Patient Involvement Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ACCURAY INCORPORATED TOMOTHERAPY HDA SYSTEM 11/20/2017
SIEMENS HEALTHCARE GMBH ONCOR IMPRESSION PLUS 11/10/2017
ELEKTA INC. MOSAIQ 11/02/2017
ELEKTA LTD XVI 10/26/2017
ELEKTA INC. MOSAIQ 10/20/2017
ELEKTA INC MOSAIQ 08/16/2017
SIEMENS HEALTHINEERS GMBH ONCOR IMPRESSION PLUS 07/21/2017
SIEMENS HEALTHINEERS GMBH LANTIS SYSTEM 06/28/2017
ACCURAY INCORPORATED TOMOEDGE TREATMENT SYSTEM 06/23/2017
MEDICAL INTELLIGENCE MEDIZINTECHNIK GMBH IGUIDE SYSTEM 06/12/2017
-
-