Skip to content

Device (Tsx-101A +3 more) - H

by Toshiba America Medical Systems, In.C

510(k) K080211

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

8 closed

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 NumberK080211 Date14 Mar 2008ClearedStatusActive

Recalls

8 recalls · FDA

    • Terminated Z-0013-2016 FDA Class II initiated 8 May 2015

    If two specific operations are performed in multi-phase helical scanning, the acquired raw data may not be saved.

    • Terminated Z-1113-2014 FDA Class II initiated 1 Oct 2013

    Toshiba intitiated this recall because their investigation revealed that due to a problem of the X-ray output control software, the X-ray output conditions may not be set correctly. As a result, X-ray exposure under the scan conditions used for contrast study may not start.

    • Terminated Z-3221-2011 FDA Unclassified (pre-2012) initiated 8 Dec 2010

    There is the potential that the current may not be controlled correctly in examinations using the ECG modulation function, which adjusts the x-ray output in synchronization with the ECG waveform.

    • Terminated Z-2204-2011 FDA Unclassified (pre-2012) initiated 9 Apr 2010

    The recall was initiated by Toshiba America Medical Systems (TAMS) because the software associated with TSX-101A: Aquilion 64 can prevent scanning from being performed at the specified helical pitch (couch movement speed).

  • 4 recalls, same reason

    • Terminated Z-1169-2010 FDA Unclassified (pre-2012) initiated 8 Jan 2009
    • Terminated Z-1166-2010 FDA Unclassified (pre-2012) initiated 8 Jan 2009
    • Terminated Z-1168-2010 FDA Unclassified (pre-2012) initiated 8 Jan 2009
    • Terminated Z-1167-2010 FDA Unclassified (pre-2012) initiated 8 Jan 2009

    Toshiba America Medical Systems Inc (TAMS) has initiated a field correction on the Aquilion 32 CT Scanners due to the potential for the bolus tracking software (SureStart) to cause delay of the helical scan, up to 10 seconds, when large volumes of data are being reconstructed on the secondary console.

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  • Withdrawn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
JAK
Device Class
Class II
Regulation
21 CFR Part 892.1750
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

Other devices from Toshiba America Medical Systems, In.C

See all devices from Toshiba America Medical Systems, In.C →