K-number	K182506
Device name	LipiScan Dynamic Meibomian Imager
Applicant	Tearscience, Inc.
Product code	HKI
Device class	Class II
Decision date	Dec 10, 2018
Decision	Substantially Equivalent
Regulation	886.1120

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Source

View the full FDA submission: accessdata.fda.gov

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LipiScan Dynamic Meibomian Imager

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