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PROCLEAR COMPATIBLES DAILY WEAR CONTACT LENS

K970095 Class II Traditional
Decision Date
1997-04-03
Sponsor / Applicant
Biocompatibles Eyewear, Inc.

Technical Specification

510(k) Submission ID K970095
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 1997-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCLEAR COMPATIBLES DAILY WEAR CONTACT LENS received FDA 510(k) clearance under submission number K970095, sponsored by Biocompatibles Eyewear, 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 1997-04-03.

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.