meddevicedb.com FDA Device Reference

CONTACT LASER & DIAGNOSTIC LENSES

K023221 Class II Special
Decision Date
2002-10-11
Sponsor / Applicant
Volk Optical, Inc.

Technical Specification

510(k) Submission ID K023221
Product Code HJK
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1385
Decision Date 2002-10-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONTACT LASER & DIAGNOSTIC LENSES received FDA 510(k) clearance under submission number K023221, sponsored by Volk Optical, 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 2002-10-11.

Classification & Regulation

This clearance is catalogued under FDA product code HJK and 21 CFR 886.1385, within the Ophthalmic review panel as a Class II device.