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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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163 records meeting your search criteria returned- Product Code: DTK Product Problem: Occlusion Within Device Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
WILLIAM COOK EUROPE UNKNOWN 09/07/2016
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 08/31/2016
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 08/26/2016
WILLIAM COOK EUROPE UNKNOWN 08/22/2016
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 08/12/2016
CORDIS CORPORATION UNKNOWN OPTEASE VENA CAVA FILTER 08/10/2016
COOK INC UNKNOWN 08/08/2016
WILLIAM COOK EUROPE COOK CELECT® PLATINUM NAVALIGN FEMORAL V 08/04/2016
WILLIAM COOK EUROPE COOK CELECT® PLATINUM NAVALIGN JUGULAR V 07/13/2016
WILLIAM COOK EUROPE COOK CELECT® PLATINUM NAVALIGN FEMORAL V 07/05/2016
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