K-number	K151102
Device name	Bausch + Lomb Injector System
Applicant	Bausch & Lomb, Inc.
Product code	MSS
Device class	Class I
Decision date	May 22, 2015
Decision	Substantially Equivalent
Regulation	886.4300

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View the full FDA submission: accessdata.fda.gov

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Bausch + Lomb Injector System

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