K-number	K963947
Device name	EPILASER NORMAL MODE RUBY LASER
Applicant	Spectrum Medical Technologies, Inc.
Product code	GEX
Device class	Class II
Decision date	Mar 5, 1997
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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EPILASER NORMAL MODE RUBY LASER

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