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CENTURION SES EPIKERATOME

K031735 Class I Traditional
Decision Date
2003-08-21
Sponsor / Applicant
Ciba Vision Corporation

Technical Specification

510(k) Submission ID K031735
Product Code HNO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4370
Decision Date 2003-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTURION SES EPIKERATOME received FDA 510(k) clearance under submission number K031735, sponsored by Ciba Vision Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2003-08-21.

Classification & Regulation

This clearance is catalogued under FDA product code HNO and 21 CFR 886.4370, within the Ophthalmic review panel as a Class I device.