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VANTAGE TITAN WITH HELIOS GRADIENT MODEL MRT-1504/US

K122613 Class II Traditional
Decision Date
2012-12-13
Sponsor / Applicant
Toshiba America Medical Systems, In.C

Technical Specification

510(k) Submission ID K122613
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2012-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VANTAGE TITAN WITH HELIOS GRADIENT MODEL MRT-1504/US received FDA 510(k) clearance under submission number K122613, 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 2012-12-13.

Classification & Regulation

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