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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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56 records meeting your search criteria returned- Product Code: DTK Product Problem: Difficult to Insert Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CORDIS US CORP. OPTEASE 03/25/2024
BARD PERIPHERAL VASCULAR, INC. DENALI JUGULAR SYSTEM 11/22/2023
BARD PERIPHERAL VASCULAR, INC. DENALI JUGULAR SYSTEM 10/26/2023
CORDIS US. CORP OPTEASE 09/01/2023
WILLIAM COOK EUROPE COOK CELECT® PLATINUM NAVALIGN FEMORAL V 03/09/2023
WILLIAM COOK EUROPE COOK CELECT® PLATINUM NAVALIGN FEMORAL V 03/07/2023
CORDIS CORPORATION OPTEASE RETR FILTER 55 FEMORAL 12/24/2022
WILLIAM COOK EUROPE GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA 12/02/2022
CORDIS CORPORATION OPTEASE RETR FILTER 55 06/24/2022
ARGON MEDICAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 03/15/2022
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