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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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8 records meeting your search criteria returned- Product Code: MLV Patient Problem: Foreign Body In Patient Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL AMPLATZER SEPTAL OCCLUDER 03/15/2024
ABBOTT MEDICAL AMPLATZER SEPTAL OCCLUDER 01/31/2024
ABBOTT MEDICAL AMPLATZER SEPTAL OCCLUDER 11/13/2023
W. L. GORE ASSOCIATES, INC. GORE CARDIOFORM SEPTAL OCCLUDER 06/01/2022
W. L. GORE & ASSOCIATES, INC. GORE CARDIOFORM ASD OCCLUDER 05/17/2021
W.L. GORE & ASSOCIATES GORE CARDIOFORM SEPTAL OCCLUDER 05/22/2017
GORE MEDICAL, W.L. GORE AND ASSOCIATES, GORE SEPTAL OCCLUDER 12/19/2016
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 10/18/2016
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