• 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 
 > 
 
194 records meeting your search criteria returned- Product Code: KRA Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 06/30/2020
BTG BOTHELL EKOSONIC KIT 106CM 12CM TZ 06/26/2020
EKOS CORPORATION EKOSONIC MACH 4 ENDOVASCULAR DEVICE 06/19/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 06/11/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 06/11/2020
MERIT MEDICAL SYSTEMS INC. MERIT MAESTRO MICROCATHETER 06/04/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 06/03/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 06/02/2020
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 10 45 PRE-SHAPED TIP 06/01/2020
MICRO THERAPEUTICS, INC. DBA EV3 REBAR 05/29/2020
-
-