K-number	K100228
Device name	VERSAPULSE MODEL P20 LASER SYSTEM
Applicant	Lumenis, Inc.
Product code	GEX
Device class	Class II
Decision date	Feb 24, 2010
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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VERSAPULSE MODEL P20 LASER SYSTEM

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