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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: DQX Patient Problem: Atrial Fibrillation Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION V-18 GUIDEWIRE (GUIDEWIRE) 08/09/2023
BOSTON SCIENTIFIC CORPORATION V-18 GUIDEWIRE (GUIDEWIRE) 08/09/2023
BOSTON SCIENTIFIC CORPORATION V-18 CONTROL WIRE 03/13/2023
VASCULAR SOLUTIONS, LLC SPECTRE GUIDEWIRE 03/10/2021
VASCULAR SOLUTIONS, LLC RAIDER GW 03/09/2021
AGA MEDICAL CORPORATION AMPLATZER GUIDEWIRE 03/18/2020
MEDTRONIC HEART VALVES DIVISION CONFIDA BRECKER CURVE GUIDEWIRE 05/29/2019
MEDTRONIC, INC. WIRE, GUIDE, CATHETER 01/16/2019
AV-TEMECULA-CT ACS HI-TORQUE BALANCE MIDDLEWEIGHT GUIDE 03/23/2018
ST. JUDE MEDICAL, COSTA RICA LTDA PRESSUREWIRE¿ 10/02/2017
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