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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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10 records meeting your search criteria returned- Product Code: LIT Patient Problem: Reocclusion Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
MEDTRONIC MEXICO ADMIRAL XTREME 09/02/2020
MEDTRONIC MEXICO PACIFIC XTREME 03/14/2020
MEDTRONIC MEXICO ADMIRAL XTREME 03/14/2020
MEDTRONIC MEXICO PACIFIC XTREME 06/04/2019
MEDTRONIC MEXICO PACIFIC PLUS 05/31/2019
COVIDIEN CHOCOLATE 05/31/2019
INVATEC SPA PACIFIC XTREME 03/15/2019
INVATEC SPA ADMIRAL XTREME 03/15/2019
COVIDIEN CHOCOLATE 02/26/2019
BOSTON SCIENTIFIC CORPORATION STERLING 01/09/2019
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