LacriJet®— 510(k) K201606

Name: FDA 510(k) clearance K201606
Creator: U.S. Food and Drug Administration
Published: 2020-12-18

Substantially Equivalent

Fci (France Chirurgie Instrumentation) Sas

FDA 510(k) clearance K201606 for LacriJet®, Substantially Equivalent on 2020-12-18. Applicant: Fci (France Chirurgie Instrumentation) Sas. Device class: Unclassified.

Clearance details

Applicant: Fci (France Chirurgie Instrumentation) Sas
Product code: Code OKS
Device class: Unclassified
Advisory panel: Unknown
Date received: 2020-06-15
Decision date: 2020-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paris, FR

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.