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DRAD30003/Radrex-I

by Toshiba America Medical Systems, In.C

510(k) K083503

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 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 NumberK083503 Date13 Feb 2009ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-0941-2012 FDA Unclassified (pre-2012) initiated 29 Dec 2011 on shared 510(k) K083503

    It has been found that some of the starter cables used for x-ray tube high speed rotation are not sufficiently durable.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

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  • Withdrawn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
KPR
Device Class
Class II
Regulation
21 CFR Part 892.1680
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

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