K-number	K120982
Device name	DIGITAL EYE-FUNDUS CAMERA
Applicant	Medimaging Integrated Solutions, Inc. (Miis)
Product code	HKI
Device class	Class II
Decision date	Sep 28, 2012
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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DIGITAL EYE-FUNDUS CAMERA

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