K-number	K043329
Device name	OMNILUX REVIVE AND BLUE
Applicant	Photo Therapeutics Limited
Product code	GEX
Device class	Class II
Decision date	Mar 18, 2005
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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OMNILUX REVIVE AND BLUE

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