meddevicedb.com FDA Device Reference

SOLO-CARE AQUA ANTIMICROBIAL LENS CASE

K041820 Class II Traditional
Decision Date
2005-09-09
Sponsor / Applicant
Ciba Vision Corporation

Technical Specification

510(k) Submission ID K041820
Product Code LRX
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 2005-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLO-CARE AQUA ANTIMICROBIAL LENS CASE received FDA 510(k) clearance under submission number K041820, sponsored by Ciba 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 2005-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code LRX and 21 CFR 886.5928, within the Ophthalmic review panel as a Class II device.