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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM-CONT 01/04/2018
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM-CONT 12/26/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/21/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/21/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/20/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/19/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/13/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/13/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/11/2017
HEARTWARE, INC. HEARTWARE VENTRICULAR ASSIST SYSTEM - CO 12/08/2017
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