K-number	K992472
Device name	SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM
Applicant	Clinicon Corp.
Product code	GEX
Device class	Class II
Decision date	Sep 8, 1999
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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SUREGUIDE CO2 LASER BEAM DELIVERY SYSTEM

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