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HORIZON 55 BI-CON TORIC

K950818 Class II Traditional
Decision Date
1995-03-21
Sponsor / Applicant
Westcon Contact Lens Co., Inc.

Technical Specification

510(k) Submission ID K950818
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 1995-03-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HORIZON 55 BI-CON TORIC received FDA 510(k) clearance under submission number K950818, sponsored by Westcon Contact Lens Co., 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 1995-03-21.

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.