K-number	K070466
Device name	REVOLIX DUO LASER SYSTEM
Applicant	Allmed Systems, Inc.
Product code	GEX
Device class	Class II
Decision date	Apr 17, 2007
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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REVOLIX DUO LASER SYSTEM

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