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

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
 

 
 
10 records meeting your search criteria returned- Product Code: KRA Patient Problem: Confusion/ Disorientation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICRO THERAPEUTICS, INC. DBA EV3 CATHERA 04/26/2024
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 02/14/2024
MICRO THERAPEUTICS, INC. DBA EV3 PHENOM 02/14/2024
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 02/14/2024
MICRO THERAPEUTICS, INC. DBA EV3 REBAR 02/14/2024
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 07/26/2023
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 07/06/2023
MICRO THERAPEUTICS, INC. DBA EV3 CATHERA 12/13/2022
MICRO THERAPEUTICS, INC. DBA EV3 CATHERA 12/13/2022
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 09/24/2021
-
-