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VELOCITY ADVANTAGE

K023939 Class II Traditional
Decision Date
2003-04-17
Sponsor / Applicant
Visioncare Devices, Inc.

Technical Specification

510(k) Submission ID K023939
Product Code HQE
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4150
Decision Date 2003-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VELOCITY ADVANTAGE received FDA 510(k) clearance under submission number K023939, sponsored by Visioncare Devices, 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 2003-04-17.

Classification & Regulation

This clearance is catalogued under FDA product code HQE and 21 CFR 886.4150, within the Ophthalmic review panel as a Class II device.