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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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5 records meeting your search criteria returned- Product Code: DTK Product Problem: Device Subassembly Report Date From: 01/1/2014
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ManufacturerBrand NameDate Report Received
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 08/27/2018
WILLIAM COOK EUROPE UNKNOWN 02/24/2016
REX MEDICAL, L.P. OPTION ELITE RETRIEVABLE VENA CAVA FILTE 06/26/2015
BARD PERIPHERAL VASCULAR, INC. MERIDIAN VENA CAVA FILTER 07/18/2014
BARD PERIPHERAL VASCULAR, INC. MERIDIAN FILTER SYSTEM 04/25/2014
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