K-number	K180378
Device name	Optomed Aurora Camera with Aurora Retinal Module and Aurora Anterior Module
Applicant	Optomed OY
Product code	HKI
Device class	Class II
Decision date	Apr 5, 2018
Decision	Substantially Equivalent
Regulation	886.1120

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Source

View the full FDA submission: accessdata.fda.gov

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Optomed Aurora Camera with Aurora Retinal Module and Aurora Anterior Module

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