KERATOREF L60— 510(k) K922253

Substantially Equivalent

Luneau Ophtalmologie SA

FDA 510(k) clearance K922253 for KERATOREF L60, Substantially Equivalent on 1992-06-19. Applicant: Luneau Ophtalmologie SA. Device class: 1.

Clearance details

Applicant: Luneau Ophtalmologie SA
Product code: Code HLQ
Device class: Class 1
Regulation: 21 CFR 886.1350
Advisory panel: Ophthalmic
Date received: 1992-05-01
Decision date: 1992-06-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chartres Cedex, FR

Download summary PDF View on FDA.gov ↗

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More clearances from Luneau Ophtalmologie SA

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