meddevicedb.com FDA Device Reference

OxyPure Color Silicone Hydrogel Soft Contact Lenses

K171447 Class II Traditional
Decision Date
2017-12-05
Sponsor / Applicant
Visco Vision, Inc.

Technical Specification

510(k) Submission ID K171447
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 2017-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OxyPure Color Silicone Hydrogel Soft Contact Lenses received FDA 510(k) clearance under submission number K171447, sponsored by Visco Vision, 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 2017-12-05.

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.