meddevicedb.com FDA Device Reference

COMFORTKONE KERATOCONUS ASPHERIC (HYBUFOCON A, FILOFILCON A, PEMUFOCON A) RIGID GAS PERMEABLE (RGP) DAILY WEAR CONTACT

K024164 Class II Traditional
Decision Date
2003-02-12
Sponsor / Applicant
Metro Optics, Inc.

Technical Specification

510(k) Submission ID K024164
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2003-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMFORTKONE KERATOCONUS ASPHERIC (HYBUFOCON A, FILOFILCON A, PEMUFOCON A) RIGID GAS PERMEABLE (RGP) DAILY WEAR CONTACT received FDA 510(k) clearance under submission number K024164, sponsored by Metro Optics, 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 2003-02-12.

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.