K-number	K822908
Device name	COHERENT FUNDUSL RETINAL CAMERA
Applicant	Coherent Medical Division
Product code	HKI
Device class	Class II
Decision date	Jan 5, 1983
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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COHERENT FUNDUSL RETINAL CAMERA

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