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SYNERGEYES HYBRID CONTACT LENSES-DAILY WEAR

K080193 Class II Traditional
Decision Date
2008-03-05
Sponsor / Applicant
Synergeyes, Inc.

Technical Specification

510(k) Submission ID K080193
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2008-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNERGEYES HYBRID CONTACT LENSES-DAILY WEAR received FDA 510(k) clearance under submission number K080193, sponsored by Synergeyes, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2008-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code HQD and 21 CFR 886.5916, within the Ophthalmic review panel as a Class II device.