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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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12 records meeting your search criteria returned- Product Code: DTK Patient Problem: Syncope Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. RECOVERY FILTER SYSTEM 03/25/2020
BARD PERIPHERAL VASCULAR, INC. G2 FILTER 03/24/2020
ARGON MEDICAL DEVICES INC. OPTION IVC FILTER 07/18/2019
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 10/08/2018
WILLIAM COOK EUROPE UNKNOWN 06/12/2018
CORDIS CASHEL 466F220B 05/22/2018
WILLIAM COOK EUROPE UNKNOWN 09/26/2017
COOK INC GUNTHER TULIP FEMORAL VENA CAVA FILTER S 09/11/2017
CORDIS CASHEL OPTEASE RETRIEVAL FILTER 09/04/2017
COOK INC UNKNOWN 08/08/2017
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