meddevicedb.com FDA Device Reference

FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES

K021738 Class II Traditional
Decision Date
2002-08-19
Sponsor / Applicant
Totoku Electric Co., Ltd.

Technical Specification

510(k) Submission ID K021738
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2002-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLAT PANEL DISPLAYS, ME SERIES & CCL SERIES received FDA 510(k) clearance under submission number K021738, sponsored by Totoku Electric Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-08-19.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.