meddevicedb.com FDA Device Reference

59% EXTREME H2O (HIOXIFILCON A) SOFT CONTACT LENS

K040303 Class II Traditional
Decision Date
2005-02-02
Sponsor / Applicant
Hydrogel Vision Corporation

Technical Specification

510(k) Submission ID K040303
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 2005-02-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

59% EXTREME H2O (HIOXIFILCON A) SOFT CONTACT LENS received FDA 510(k) clearance under submission number K040303, sponsored by Hydrogel 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 2005-02-02.

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.