LacriJet®
K-Number: K201606 · 2020-12-18
Device Summary
Frequently Asked Questions
What is the LacriJet®?
LacriJet® is a medical device that received FDA 510(k) clearance on 2020-12-18. The listed applicant is Fci (France Chirurgie Instrumentation) Sas. The 510(k) number is K201606.
When did LacriJet® receive FDA 510(k) clearance?
LacriJet® received FDA 510(k) clearance on 2020-12-18, under 510(k) number K201606.
Who is the listed applicant for LacriJet®?
The FDA 510(k) record lists Fci (France Chirurgie Instrumentation) Sas as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LacriJet®?
The FDA product code for LacriJet® is OKS.
Other records listing Fci (France Chirurgie Instrumentation) Sas as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OKS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.