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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
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
EKOS CORPORATION CATHETER, CONTINUOUS FLUSH 11/08/2019
BOSTON SCIENTIFIC CORPORATION ANGIOJET ZELANTE DVT 10/31/2019
COOK INC TRIFORCE¿ PERIPHERAL CROSSING SET 10/23/2019
MICRO THERAPEUTICS, INC. DBA EV3 ECHELON 10/22/2019
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 10/22/2019
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN 10/21/2019
COOK INC MIRA-FLEX MICROCATHETER 10/18/2019
MICRO THERAPEUTICS, INC. DBA EV3 MARKSMAN CATHETER 10/16/2019
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 10/16/2019
MICRO THERAPEUTICS, INC. DBA EV3 MARATHON 10/14/2019
-
-