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

MAUDE - Manufacturer and User Facility Device Experience
  • 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 
 > 
 
14 records meeting your search criteria returned- Product Code: KRA Product Problem: No Apparent Adverse Event Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICRO THERAPEUTICS, INC. DBA EV3 CATHERA 10/04/2022
MICRO THERAPEUTICS, INC. DBA EV3 PHENOM 09/16/2022
MICRO THERAPEUTICS, INC. DBA EV3 CATHERA 08/11/2022
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 06/30/2022
MICRO THERAPEUTICS, INC. DBA EV3 CRAGG-MCNAMARA 04/20/2022
MICRO THERAPEUTICS, INC. DBA EV3 PHENOM 04/18/2022
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 04/08/2022
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 02/26/2022
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 02/06/2022
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 01/19/2022
-
-