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Vantage Titan 1.5T, MRT-1510, M-Power GX

by Toshibamedical Systems Corporation

510(k) K170412

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

2 ongoing

This device is named in the recall

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK170412 Date7 Jun 2017ClearedStatusActive

Recalls

2 recalls · 2 ongoing · FDA

    • Ongoing Z-2045-2021 FDA Class II initiated 21 May 2021

    The MRI system contains a component that does not meet the appropriate flame retardancy-rating which could result in smoke or fire.

    • Ongoing Z-0199-2019 FDA Class II initiated 30 May 2018

    When using respiratory gating with Steady Mode ON in Spin Echo sequence scanning, the SAR (Specific Absorption Rate) value displayed on the console may be lower than the actual SAR value. The actual applied SAR values may exceed the FIRST LEVEL CONTROLLED OPERATING MODE.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
LNH
Device Class
Class II
Regulation
21 CFR Part 892.1000
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

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