K-number	K213592
Device name	Iridex 810 Laser
Applicant	Iridex Corporation
Product code	HQF
Device class	Class II
Decision date	Mar 23, 2022
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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Iridex 810 Laser

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