• 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
 

 
 
7 records meeting your search criteria returned- Product Code: KRA Patient Problem: Visual Impairment Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 11/14/2023
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 11/14/2023
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 10/02/2023
MICRO THERAPEUTICS, INC. DBA EV3 PHENOM 09/29/2023
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 08/23/2023
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 07/20/2023
MICRO THERAPEUTICS, INC. DBA EV3 NV MICROCATHETER 02/22/2022
-
-