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QD KNEE/FOOT COIL, MODEL MJQJ-147A

K051763 Class II Traditional
Decision Date
2005-07-14
Sponsor / Applicant
Toshiba America Medical Systems, In.C

Technical Specification

510(k) Submission ID K051763
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2005-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QD KNEE/FOOT COIL, MODEL MJQJ-147A received FDA 510(k) clearance under submission number K051763, sponsored by Toshiba America Medical Systems, In.C. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-07-14.

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.