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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
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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 02/28/2018
CORDIS CASHEL UNKNOWN OPTEASE RETREIVABLE VENA CAVA FI 02/22/2018
BARD PERIPHERAL VASCULAR, INC. ECLIPSE FILTER SYSTEM - FEMORAL 02/14/2018
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 02/09/2018
CORDIS CASHEL 466P306X 01/29/2018
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 01/23/2018
COOK INC UNKNOWN 12/28/2017
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 12/26/2017
BARD PERIPHERAL VASCULAR, INC. MERIDIAN FILTER SYSTEM - JUGULAR 12/21/2017
BARD PERIPHERAL VASCULAR, INC. DENALI JUGULAR SYSTEM 12/21/2017
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