K-number	K963389
Device name	FLEX-LASE 600 SERIES ION LASER SYSTEM
Applicant	American Laser Medical
Product code	GEX
Device class	Class II
Decision date	Nov 26, 1996
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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FLEX-LASE 600 SERIES ION LASER SYSTEM

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