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Stereotaxis Inc submits 510(k) application to FDA for Vdrive with V-CAS Catheter Advancement System

Tuesday, 10 Jun 2014 06:30am EDT 

Stereotaxis Inc:Submitted a 510(k) Premarket notification to Food and Drug Administration (FDA) for company's Vdrive Robotic Navigation System with V-CAS Catheter Advancement System.Submission follows company's 510(k) application for Vdrive with V-Loop Variable Loop Catheter Manipulator on March 31, includes both the single-arm system (Vdrive) and two-arm system (Vdrive Duo). 

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