K-number	K113500
Device name	CANADY VIEIRA HYBRID PLASMA SCALPEL
Applicant	Us Medical Innovations, LLC
Product code	GEI
Device class	Class II
Decision date	Dec 9, 2011
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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CANADY VIEIRA HYBRID PLASMA SCALPEL

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