K-number	K103547
Device name	LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEM
Applicant	Lightmed Corp.
Product code	HQF
Device class	Class II
Decision date	Nov 3, 2011
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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LIGHTLAS MULTI-WAVELENGTH MEDICAL LASER SYSTEM

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