K-number	K992298
Device name	IRIDERM, MODEL APEX 800
Applicant	Iridex Corp
Product code	GEX
Device class	Class II
Decision date	Dec 9, 1999
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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IRIDERM, MODEL APEX 800

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