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HORIZON EPIKERATOME DISPOSABLE MICROKERATOME SYSTEM

K052891 Class I Traditional
Decision Date
2006-03-23
Sponsor / Applicant
Hawken Industries

Technical Specification

510(k) Submission ID K052891
Product Code HNO
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4370
Decision Date 2006-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HORIZON EPIKERATOME DISPOSABLE MICROKERATOME SYSTEM received FDA 510(k) clearance under submission number K052891, sponsored by Hawken Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2006-03-23.

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.