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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
BARD PERIPHERAL VASCULAR, INC. MERIDIAN FILTER SYSTEM - JUGULAR 10/20/2017
CORDIS CASHEL 466FXXXX 10/20/2017
WILLIAM COOK EUROPE COOK CELECT FEMORAL VENA CAVA FILTER SET 10/20/2017
CORDIS CASHEL UNKNOWN OPTEASE RETREIVABLE VENA CAVA FI 10/16/2017
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 09/28/2017
CORDIS CASHEL 466FXXXX 09/22/2017
BARD PERIPHERAL VASCULAR, INC. DENALI JUGULAR SYSTEM 09/15/2017
BARD PERIPHERAL VASCULAR, INC. MERIDIAN FILTER SYSTEM - FEMORAL 09/15/2017
CORDIS CASHEL UNKNOWN OPTEASE RETREIVABLE VENA CAVA FI 09/06/2017
CORDIS CASHEL 466FXXXX 09/03/2017
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