• 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 
 > 
 
46 records meeting your search criteria returned- Product Code: DTK Product Problem: Complete Blockage Report Date From: 01/1/2014
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS CORPORATION FILTER, INTRAVASCULAR, CARDIOVASCULAR 12/21/2020
ARGON MEDICAL DEVICES, INC. OPTION ELITE RETRIEVABLE VENA CAVA FILTE 09/18/2020
ARGON MEDICAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 06/02/2020
CORDIS CASHEL 466FXXXX 07/03/2019
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 04/24/2019
CORDIS CASHEL 466P306X 01/30/2019
CORDIS CASHEL 466FXXXX 01/30/2019
CORDIS CASHEL 466FXXXX 01/30/2019
CORDIS CASHEL 466P306X 01/10/2019
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER. 08/28/2018
-
-