K-number	K970667
Device name	NUVO-LASE 660 LASER SYSTEM
Applicant	American Laser Medical
Product code	GEX
Device class	Class II
Decision date	May 13, 1997
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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NUVO-LASE 660 LASER SYSTEM

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