• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
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
CATHERA, INC. PHENOM CATHETER 03/09/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 03/04/2020
COOK INC CXI SUPPORT CATHETER 03/02/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 03/02/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 02/28/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 165 AVM CATHETER 02/27/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 02/27/2020
ARGON MEDICAL DEVICES CLEANER XT ROTATIONAL THROMBECTOMY SYSTE 02/26/2020
ARGON MEDICAL DEVICES INC. CLEANER15 ROTATIONAL THROMBECTOMY SYSTEM 02/19/2020
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 02/12/2020
-
-