K-number	K002920
Device name	MEGAVISION CPX, MEGAVISION FA, MODEL I AND II
Applicant	Escalon Medical Corp.
Product code	HKI
Device class	Class II
Decision date	Dec 18, 2000
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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MEGAVISION CPX, MEGAVISION FA, MODEL I AND II

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