K-number	K230627
Device name	Zilia Ocular FC (ZIL-10002)
Applicant	Zilia, Inc.
Product code	HKI
Device class	Class II
Decision date	Nov 20, 2023
Decision	Substantially Equivalent
Regulation	886.1120

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View the full FDA submission: accessdata.fda.gov

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Zilia Ocular FC (ZIL-10002)

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