K-number	K170470
Device name	Digital Eye Anterior Camera
Applicant	Medimaging Integrated Solution, Inc (Miis)
Product code	HJO
Device class	Class II
Decision date	Oct 6, 2017
Decision	Substantially Equivalent
Regulation	886.1850

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Source

View the full FDA submission: accessdata.fda.gov

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Digital Eye Anterior Camera

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