K-number	K954842
Device name	D.O.R.C. VFI/VFE SYSTEM
Applicant	Dutch Ophthalmic USA, Inc.
Product code	KYG
Device class	Class I
Decision date	Apr 15, 1996
Decision	Substantially Equivalent
Regulation	886.4360

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D.O.R.C. VFI/VFE SYSTEM

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