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PROCLEAR (OMAFILCON A) SOFT HYDROPHILIC) CONTACT LENS

K123202 Class II Special
Decision Date
2013-05-30
Sponsor / Applicant
CooperVision, Inc.

Technical Specification

510(k) Submission ID K123202
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 2013-05-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROCLEAR (OMAFILCON A) SOFT HYDROPHILIC) CONTACT LENS received FDA 510(k) clearance under submission number K123202, sponsored by CooperVision, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2013-05-30.

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.