K-number	K173480
Device name	Crystalsert Lens Delivery System
Applicant	Bausch & Lomb, Inc.
Product code	MSS
Device class	Class I
Decision date	Dec 11, 2017
Decision	Substantially Equivalent
Regulation	886.4300

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Source

View the full FDA submission: accessdata.fda.gov

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Crystalsert Lens Delivery System

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