K-number	K230785
Device name	Precision1, Precision1 for Astigmatism
Applicant	Alcon Laboratories, Inc.
Product code	LPL
Device class	Class II
Decision date	Apr 20, 2023
Decision	Substantially Equivalent
Regulation	886.5925

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Source

View the full FDA submission: accessdata.fda.gov

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Precision1, Precision1 for Astigmatism

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