K-number	K050223
Device name	VIVAWAVE MICROWAVE ABLATION SYSTEM, COAXIAL INTRODUCER
Applicant	Vivant Medical, Inc.
Product code	GEI
Device class	Class II
Decision date	Feb 24, 2005
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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VIVAWAVE MICROWAVE ABLATION SYSTEM, COAXIAL INTRODUCER

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