K-number	K884960
Device name	ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL
Applicant	Bausch & Lomb Pharmaceutical, Inc.
Product code	MOE
Device class	Class I
Decision date	Feb 13, 1989
Decision	Substantially Equivalent
Regulation	886.4750

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ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL

Everything you need for a 510(k) submission. Nothing you don't.