K-number	K013232
Device name	CYBERCASES BY BAUSCH & LOMB
Applicant	Bausch & Lomb, Inc.
Product code	LRX
Device class	Class II
Decision date	Nov 20, 2001
Decision	Substantially Equivalent
Regulation	886.5928

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View the full FDA submission: accessdata.fda.gov

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CYBERCASES BY BAUSCH & LOMB

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