K-number	K102412
Device name	VISTA DIGITAL OPTHALMOSCOPE
Applicant	Eyequick.Llc
Product code	HKI
Device class	Class II
Decision date	Jun 23, 2011
Decision	Substantially Equivalent
Regulation	886.1120

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Source

View the full FDA submission: accessdata.fda.gov

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VISTA DIGITAL OPTHALMOSCOPE

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