FDA 510(k), K113500, CANADY VIEIRA HYBRID PLASMA SCALPEL

FDA 510(k), K113500, CANADY VIEIRA HYBRID PLASMA SCALPEL

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510(K) Number: K113500
Device Name: CANADY VIEIRA HYBRID PLASMA SCALPEL
Manufacturer:
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: 878.4400
Classification Product Code: GEI
Date Received: 11/25/2011
Decision Date: 12/09/2011
Regulation Medical Specialty: General & Plastic Surgery
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