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DAILY WEAR SOFT (HYDROPHILIC) CONTACT LENS

K953807 Class II Traditional
Decision Date
1996-02-14
Sponsor / Applicant
Stephen A. Dunn, Inc.

Technical Specification

510(k) Submission ID K953807
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 1996-02-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DAILY WEAR SOFT (HYDROPHILIC) CONTACT LENS received FDA 510(k) clearance under submission number K953807, sponsored by Stephen A. Dunn, 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 1996-02-14.

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.