K-number	K223357
Device name	EyeArt v2.2.0
Applicant	Eyenuk, Inc.
Product code	PIB
Device class	Class II
Decision date	Jun 16, 2023
Decision	Substantially Equivalent
Regulation	886.1100

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Source

View the full FDA submission: accessdata.fda.gov

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EyeArt v2.2.0

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