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
 

 
 
7 records meeting your search criteria returned- Product Code: DXE Patient Problem: Vessel Or Plaque, Device Embedded In Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LEMAITRE VASCULAR, INC. SINGLE LUMEN EMBOLECTOMY CATHETER 10/18/2019
EDWARDS LIFESCIENCES, PR FOGARTY ARTERIAL EMBOLECTOMY CATHETER 08/12/2019
LEMAITRE VASCULAR, INC. OVER-THE-WIRE EMBOLECTOMY CATHETER 08/08/2019
VASCULAR SOLUTIONS, LLC PRONTO LP 04/18/2019
VASCULAR SOLUTIONS, LLC PRONTO LP 04/03/2019
TELEFLEX INCORPORATED ARROW-TREROTOLA PTD 03/19/2019
ARROW INTERNATIONAL INC. ARROW PERCUTANEOUS THROMBOLYTIC DEVICE K 01/16/2019
-
-