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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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184 records meeting your search criteria returned- Product Code: DTK Product Problem: Occlusion Within Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. DENALI FEMORAL SYSTEM 12/19/2017
COOK INC GUNTHER TULIP FEMORAL VENA CAVA FILTER S 12/18/2017
BARD PERIPHERAL VASCULAR, INC. RECOVERY FILTER SYSTEM 12/18/2017
WILLIAM COOK EUROPE GUNTHER TULIP NAVALIGN JUGULAR VENA CAVA 12/15/2017
BARD PERIPHERAL VASCULAR, INC. G2 FILTER SYSTEM - FEMORAL 12/13/2017
CORDIS CASHEL 466FXXXX 12/12/2017
CORDIS CASHEL 466FXXXX 12/12/2017
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 12/12/2017
BARD PERIPHERAL VASCULAR, INC. G2 FILTER SYSTEM - JUGULAR 12/11/2017
BARD PERIPHERAL VASCULAR, INC. MERIDIAN FILTER SYSTEM - FEMORAL 12/07/2017
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