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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
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 01/30/2017
BARD PERIPHERAL VASCULAR, INC. DENALI FEMORAL SYSTEM 01/20/2017
WILLIAM COOK EUROPE GÜNTHER TULIP VENA CAVA FILTER JUGULAR A 01/20/2017
BARD PERIPHERAL VASCULAR, INC. G2 FILTER SYSTEM - FEMORAL 01/19/2017
BARD PERIPHERAL VASCULAR, INC. RECOVERY FILTER SYSTEM 01/17/2017
BARD PERIPHERAL VASCULAR, INC. DENALI FILTER SYSTEM 01/05/2017
BARD PERIPHERAL VASCULAR, INC. MERIDIAN FILTER SYSTEM - FEMORAL 12/21/2016
WILLIAM COOK EUROPE COOK CELECT JUGULAR VENA CAVA FILTER SET 12/21/2016
WILLIAM COOK EUROPE UNKNOWN 12/16/2016
COOK INC GUNTHER TULIP JUGULAR VENA CAVA FILTER S 12/02/2016
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