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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 - FEMORAL 08/31/2017
BARD PERIPHERAL VASCULAR, INC. G2 FILTER SYSTEM - FEMORAL 08/30/2017
BARD PERIPHERAL VASCULAR, INC. VENA CAVA FILTER SYSTEM 08/28/2017
CORDIS CASHEL OPTEASE FEMORAL 55 CM KIT 08/21/2017
WILLIAM COOK EUROPE GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA 08/11/2017
BARD PERIPHERAL VASCULAR, INC. ECLIPSE FILTER SYSTEM - JUGULAR 08/02/2017
CORDIS CASHEL LTD. 466FXXXX 07/18/2017
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 07/18/2017
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 07/18/2017
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 07/03/2017
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