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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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131 records meeting your search criteria returned- Product Code: DSQ Product Problem: Occlusion Within Device Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
THORATEC CORPORATION HEARTMATE II LVAD 05/04/2015
THORATEC CORPORATION HEARTMATE II LVAS 04/14/2015
THORATEC CORPORATION HEARTMATE II LVAS 04/10/2015
HEARTWARE, INC. HEARTWARE HVAD 04/09/2015
THORATEC CORPORATION HEARTMATE II LVAS 04/09/2015
HEARTWARE, INC HEARTWARE® VENTRICULAR ASSIST SYSTEM 04/07/2015
THORATEC CORPORATION HEARTMATE II LVAS 03/18/2015
HEARTWARE, INC. HEARTWARE HVAD 03/13/2015
THORATEC CORPORATION HEARTMATE II LVAS 03/11/2015
HEARTWARE, INC. HEARTWARE HVAD 03/11/2015
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