K-number	K170322
Device name	Catalys Precision Laser System
Applicant	Abbott Medical Optics, Inc.
Product code	OOE
Device class	Class II
Decision date	May 19, 2017
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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Catalys Precision Laser System

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