K-number	K023111
Device name	GYRUS PLASMA SKIN RESURFACING SYSTEM
Applicant	Gyrus Medical, Inc.
Product code	GEI
Device class	Class II
Decision date	Mar 13, 2003
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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GYRUS PLASMA SKIN RESURFACING SYSTEM

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