LacriJet®
K-Number: K201606 · 2020-12-18
Decision Date2020-12-18
Product CodeOKS
DecisionSubstantially Equivalent
Device Summary
LacriJet® is a medical device manufactured by Fci (France Chirurgie Instrumentation) Sas. It received FDA 510(k) clearance on 2020-12-18 under approval number K201606. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LacriJet®?
LacriJet® is a medical device that received FDA 510(k) clearance on 2020-12-18. It is manufactured by Fci (France Chirurgie Instrumentation) Sas. The 510(k) number is K201606.
When was LacriJet® approved by the FDA?
LacriJet® received FDA 510(k) clearance on 2020-12-18, under approval number K201606.
What company makes LacriJet®?
LacriJet® is manufactured by Fci (France Chirurgie Instrumentation) Sas.
What is the FDA product code for LacriJet®?
The FDA product code for LacriJet® is OKS.
Other Devices by Fci (France Chirurgie Instrumentation) Sas
Related Devices (Code: OKS)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.