meddevicedb.com FDA Device Reference

VASSEN COLOR

K141699 Class II Traditional
Decision Date
2014-10-07
Sponsor / Applicant
Vassen Co., Ltd.

Technical Specification

510(k) Submission ID K141699
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 2014-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VASSEN COLOR received FDA 510(k) clearance under submission number K141699, sponsored by Vassen Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2014-10-07.

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.