meddevicedb.com FDA Device Reference

TR BAND

K070423 Class II Traditional
Decision Date
2007-03-28
Sponsor / Applicant
Terumo Medical Corp.

Technical Specification

510(k) Submission ID K070423
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 2007-03-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TR BAND received FDA 510(k) clearance under submission number K070423, sponsored by Terumo Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-03-28.

Classification & Regulation

This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.