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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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82 records meeting your search criteria returned- Product Code: DTK Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2014
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ManufacturerBrand NameDate Report Received
CORDIS CASHEL 466FXXXX 06/27/2018
CORDIS CASHEL OPTEASE FILTER 04/18/2018
COOK INC GUNTHER TULIP JUGULAR VENA CAVA FILTER S 04/16/2018
COOK MEDICAL LLC COOK MEDICAL 03/22/2018
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 01/05/2018
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 12/15/2017
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 09/19/2017
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 06/15/2017
COOK INC UNKNOWN 05/24/2017
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 04/25/2017
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