K-number	K080180
Device name	MODIFICATION TO RETINAL FUNCTION IMAGER (RFI)
Applicant	Optical Imaging , Ltd.
Product code	HKI
Device class	Class II
Decision date	Jun 11, 2008
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO RETINAL FUNCTION IMAGER (RFI)

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