FDA 510(k), K162914, VenaCure EVLT NeverTouch Procedure Kit

FDA 510(k), K162914, VenaCure EVLT NeverTouch Procedure Kit

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510(K) Number: K162914
Device Name: VenaCure EVLT NeverTouch Procedure Kit
Manufacturer: AngioDynamics, Inc.
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 10/17/2016
Decision Date: 11/16/2016
Regulation Medical Specialty: General & Plastic Surgery

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