FDA 510(k), K143536, Voyant Fine Fusion Device

FDA 510(k), K143536, Voyant Fine Fusion Device

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510(K) Number: K143536
Device Name: Voyant Fine Fusion Device
Manufacturer: APPLIED MEDICAL RESOURCES
Device Classification Name: electrosurgical, cutting & coagulation & accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 12/15/2014
Decision Date: 04/16/2015
Regulation Medical Specialty: General & Plastic Surgery

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