K-number	K033259
Device name	LIGHT AGE Q-CLEAR LASER, MODEL 701-1101
Applicant	Light Age, Inc.
Product code	GEX
Device class	Class II
Decision date	Feb 25, 2004
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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LIGHT AGE Q-CLEAR LASER, MODEL 701-1101

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