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TOSHIBA 3T EXTRA LARGE KNEE COIL

K112313 Class II Special
Decision Date
2011-09-09
Sponsor / Applicant
Quality Electrodynamics

Technical Specification

510(k) Submission ID K112313
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2011-09-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOSHIBA 3T EXTRA LARGE KNEE COIL received FDA 510(k) clearance under submission number K112313, sponsored by Quality Electrodynamics. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-09-09.

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.