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Hansen Medical Announces FDA Conditional IDE Approval for Evaluating Sensei X Robotic Catheter System for Treatment of Atrial Fibrillation
MOUNTAIN VIEW, CA, May 12, 2010 (MARKETWIRE via COMTEX) --Hansen Medical, Inc. (NASDAQ: HNSN) announced that it has received conditional Investigational Device Exemption (IDE) approval from the U.S. Food & Drug Administration (FDA) authorizing a clinical trial to investigate use of the Sensei(R) X Robotic Catheter System and the Artisan(TM) Control Catheter for treatment of Atrial Fibrillation (AF).