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REVITALEYES, POST-SURGICAL SOFT DAILY WEAR CONTACT LENS (HIOXIFILCON B) CLEAR AND BLUE VISIBILITY TINT

K080512 Class II Traditional
Decision Date
2008-07-23
Sponsor / Applicant
Metro Optics of Austin, Inc.

Technical Specification

510(k) Submission ID K080512
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 2008-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REVITALEYES, POST-SURGICAL SOFT DAILY WEAR CONTACT LENS (HIOXIFILCON B) CLEAR AND BLUE VISIBILITY TINT received FDA 510(k) clearance under submission number K080512, sponsored by Metro Optics of Austin, 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 2008-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code LPL and 21 CFR 886.5925, within the Ophthalmic review panel as a Class II device.