• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
 
163 records meeting your search criteria returned- Product Code: DTK Product Problem: Occlusion Within Device Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. G2 X FILTER SYSTEM - FEMORAL 11/29/2016
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 11/22/2016
WILLIAM COOK EUROPE UNKNOWN 11/17/2016
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 11/10/2016
BARD PERIPHERAL VASCULAR INC. SIMON NITINOL FILTER 11/06/2016
CORDIS CORPORATION 466FXXXX 11/03/2016
CORDIS CORPORATION 466FXXXX 10/31/2016
WILLIAM COOK EUROPE COOK CELECT FEMORAL VENA CAVA FILTER SET 10/11/2016
COOK INC GUNTHER TULIP FEMORAL VENA CAVA FILTER S 09/28/2016
WILLIAM COOK EUROPE COOK CELECT® PLATINUM NAVALIGN UNISET VE 09/09/2016
-
-