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GAITHERSBURG, Md.----Biosense Webster, Inc., a Johnson & Johnson company, today reported the Circulatory System Devices Panel of the U.S. Food and Drug Administration unanimously recommended approval of the Company’s Pre-Market Approval supplement for the NAVISTAR® THERMOCOOL® Catheter for the treatment of symptomatic paroxysmal atrial fibrillation.
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FDA Advisory Panel Unanimously Recommends Approval of NAVISTAR ... - Businesswire.com
GAITHERSBURG, Md.--( BUSINESS WIRE )--Biosense Webster, Inc., a Johnson & Johnson company, today reported the Circulatory System Devices Panel of the U.S. Food and Drug Administration (FDA) unanimously recommended approval of the Company?s Pre ...
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Biosense Webster, Inc., a Johnson & Johnson company, today reported the Circulatory System Devices Panel of the U.S. Food and Drug Administration (FDA) unanimously recommended approval of the Company"s Pre-Market Approval (PMA) supplement for the ...
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