K-number	K173365
Device name	Bausch + Lomb Boston Scleral Lens Case
Applicant	Bausch & Lomb, Incorporated
Product code	LRX
Device class	Class II
Decision date	Nov 17, 2017
Decision	Substantially Equivalent
Regulation	886.5928

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Source

View the full FDA submission: accessdata.fda.gov

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Bausch + Lomb Boston Scleral Lens Case

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