K-number	K020374
Device name	OCULIGHT SL/SLX
Applicant	Iridex Corp
Product code	HQF
Device class	Class II
Decision date	May 3, 2002
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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OCULIGHT SL/SLX

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