K-number	K990725
Device name	NUVOLASE 532 LASER SYSTEM
Applicant	American Laser Corp.
Product code	GEX
Device class	Class II
Decision date	Mar 22, 1999
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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NUVOLASE 532 LASER SYSTEM

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