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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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97 records meeting your search criteria returned- Product Code: LIT Patient Problem: Patient Problem/Medical Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
COVIDIEN POWERCROSS 018 02/28/2017
MEDTRONIC MEXICO ADMIRAL XTREME OTW 02/08/2017
COVIDIEN UNKNOWN PTA BALLOON 02/01/2017
INVATEC SPA REEF HP 01/19/2017
COVIDIEN FORTREX 0.035 OTW PTA BALLOON CATHETER 01/17/2017
COVIDIEN EVERCROSS 035 01/12/2017
COVIDIEN POWERCROSS 018 01/12/2017
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