• 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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
156 records meeting your search criteria returned- Product Code: DTK Product Problem: Occlusion Within Device Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 07/04/2018
CORDIS CASHEL UNKNOWN OPTEASE VENA CAVA FILTER 06/26/2018
CORDIS CASHEL UNKNOWN OPTEASE VENA CAVA FILTER 06/26/2018
CORDIS CASHEL 466F220A 06/21/2018
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 06/21/2018
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 06/01/2018
CORDIS CASHEL 466P306X 05/31/2018
COOK INC GUNTHER TULIP JUGULAR & FEMORAL VENA CAV 05/30/2018
WILLIAM COOK EUROPE COOK CELECT NAVALIGN JUGULAR & FEMORAL V 05/30/2018
BARD PERIPHERAL VASCULAR, INC. DENALLI JUGULAR SYSTEM 05/18/2018
-
-