K-number	K954781
Device name	KOWA GENESIS HAND-HELD FUNDUS CAMERA
Applicant	Kowa Optimed, Inc.
Product code	HKI
Device class	Class II
Decision date	Dec 1, 1995
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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KOWA GENESIS HAND-HELD FUNDUS CAMERA

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