Skip to content

Vantage Titan 3T, MRT-3010/A7, M-Power GX

by Toshiba Medical Systems Corporation, Japan

510(k) K172878

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 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 NumberK172878 Date17 Nov 2017ClearedStatusActive

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-2046-2021 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.

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  • Withdrawn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

Other devices from Toshiba Medical Systems Corporation, Japan

See all devices from Toshiba Medical Systems Corporation, Japan →