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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 LVAS 01/15/2017
HEARTWARE, INC HEARTWARE® VENTRICULAR ASSIST SYSTEM 01/12/2017
THORATEC CORPORATION HEARTMATE II LVAS 12/29/2016
THORATEC CORPORATION HEARTMATE 2 12/02/2016
THORATEC CORPORATION HEARTMATE II LVAS 11/30/2016
HEARTWARE, INC HEARTWARE® VENTRICULAR ASSIST SYSTEM 10/30/2016
ST JUDE (FORMERLYTHORATEC) HEARTMATE II LVAS 10/28/2016
HEARTWARE, INC HEARTWARE® VENTRICULAR ASSIST SYSTEM 10/19/2016
THORATEC HEARTMATE II 09/19/2016
THORATEC CORPORATION HEARTMATE II LVAS 08/24/2016
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