K-number	K040005
Device name	PROFILE 2000/3000 LASER SYSTEM
Applicant	Sciton, Inc
Product code	GEX
Device class	Class II
Decision date	Mar 29, 2004
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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PROFILE 2000/3000 LASER SYSTEM

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