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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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18 records meeting your search criteria returned- Product Code: MLV Product Problem: Malposition of Device Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 11/08/2018
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 08/24/2017
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 11/23/2015
AGA MEDICAL CORPORATION AMPLATZER DUCT OCCLUDER II 10/20/2015
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 01/28/2015
W.L. GORE & ASSOCIATES GORE HELEX SEPTAL OCCLUDER 07/28/2014
W.L. GORE & ASSOCIATES GORE HELEX SEPTAL OCCLUDER 07/23/2014
W.L. GORE AND ASSOCIATES, INC. HELEX ATRIAL SEPTAL OCCLUDER 01/17/2014
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