K-number	K812896
Device name	I.V.E. REFRACTION SYSTEM
Applicant	Bausch & Lomb, Inc.
Product code	HKO
Device class	Class I
Decision date	Dec 2, 1981
Decision	Substantially Equivalent
Regulation	886.1760

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View the full FDA submission: accessdata.fda.gov

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I.V.E. REFRACTION SYSTEM

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