K-number	K020849
Device name	APEX 800 LASER SYSTEM, MODEL APEX 800
Applicant	Iridex Corp
Product code	GEX
Device class	Class II
Decision date	May 20, 2002
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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APEX 800 LASER SYSTEM, MODEL APEX 800

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