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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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13 records meeting your search criteria returned- Product Code: MLV Product Problem: Entrapment of Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM ASD OCCLUDER 01/19/2024
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM ASD OCCLUDER 10/16/2023
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM ASD OCCLUDER 08/02/2023
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM ASD OCCLUDER 07/10/2023
W. L. GORE & ASSOCIATES, INC. GORE CARDIOFORM SEPTAL OCCLUDER 11/24/2020
AGA MEDICAL CORPORATION AMPLATZER 11/27/2019
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 07/25/2018
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 04/16/2018
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 08/30/2017
AGA MEDICAL CORPORATION AMPLATZER MUSCULAR VSD OCCLUDER 12/08/2015
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