meddevicedb.com FDA Device Reference

TOSHIBA 3T 32CH HEAD SPEEDER COIL,

K122638 Class II Traditional
Decision Date
2012-09-25
Sponsor / Applicant
Quality Electrodynamics

Technical Specification

510(k) Submission ID K122638
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2012-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOSHIBA 3T 32CH HEAD SPEEDER COIL, received FDA 510(k) clearance under submission number K122638, sponsored by Quality Electrodynamics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.