K-number	K032191
Device name	OMNILIGHT FLUORESCENT PULSED LIGHT SYSTEM
Applicant	Luxsano AB
Product code	GEX
Device class	Class II
Decision date	Aug 20, 2003
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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OMNILIGHT FLUORESCENT PULSED LIGHT SYSTEM

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