meddevicedb.com FDA Device Reference

DAILY WEAR SOFT CONTACT LENSES

K941484 Class II Traditional
Decision Date
1994-06-09
Sponsor / Applicant
Ciba Vision Corporation

Technical Specification

510(k) Submission ID K941484
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 1994-06-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DAILY WEAR SOFT CONTACT LENSES received FDA 510(k) clearance under submission number K941484, 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 1994-06-09.

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.