K-number	K090466
Device name	DIGITAL RETINAL CAMERA, CR-1 MARK II
Applicant	Canon, Inc.
Product code	HKI
Device class	Class II
Decision date	Mar 23, 2009
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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DIGITAL RETINAL CAMERA, CR-1 MARK II

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