LUNEAU STERILE TONOMETER SEPARATION PRISMS— 510(k) K023838

Name: FDA 510(k) clearance K023838
Creator: U.S. Food and Drug Administration
Published: 2003-02-20

Substantially Equivalent

Luneau SA

FDA 510(k) clearance K023838 for LUNEAU STERILE TONOMETER SEPARATION PRISMS, Substantially Equivalent on 2003-02-20. Applicant: Luneau SA. Device class: 2.

Clearance details

Applicant: Luneau SA
Product code: Code HKY
Device class: Class 2
Regulation: 21 CFR 886.1930
Advisory panel: Ophthalmic
Date received: 2002-11-18
Decision date: 2003-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chartres Cedex, FR

Download summary PDF View on FDA.gov ↗

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