K-number	K100384
Device name	FIBERLASE C02 LASER WAVEGUIDE
Applicant	Lumenis, Ltd.
Product code	GEX
Device class	Class II
Decision date	Apr 12, 2010
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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FIBERLASE C02 LASER WAVEGUIDE

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