K-number	K201606
Device name	LacriJet®
Applicant	Fci (France Chirurgie Instrumentation) Sas
Product code	OKS
Device class	Class U
Decision date	Dec 18, 2020
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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LacriJet®

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