• 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 
 > 
 
47 records meeting your search criteria returned- Product Code: DTK Patient Problem: Unspecified Tissue Injury Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS CORPORATION UNKNOWN TRAPEASE 08/10/2021
CORDIS CORPORATION UNKNOWN TRAPEASE 08/09/2021
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 07/30/2021
CORDIS CORPORATION UNKNOWN TRAPEASE 07/29/2021
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 07/26/2021
CORDIS CORPORATION UNKNOWN VENA CAVA FILTER 07/23/2021
CORDIS CORPORATION OPTEASE RETRIEVAL FILTER 07/22/2021
CORDIS CORPORATION TRAPEASE PVCF FEM/JUG 55CM CSI 07/22/2021
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 07/15/2021
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 07/12/2021
-
-