FDA 510(k), K070216, VARI-LASE BRIGHT TIP FIBER

FDA 510(k), K070216, VARI-LASE BRIGHT TIP FIBER

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510(K) Number: K070216
Device Name: VARI-LASE BRIGHT TIP FIBER
Manufacturer: VASCULAR SOLUTIONS, INC.
Device Classification Name: Powered Laser Surgical Instrument
Regulation Number: 878.4810
Classification Product Code: GEX
Date Received: 01/23/2007
Decision Date: 03/16/2007
Regulation Medical Specialty: General & Plastic Surgery

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