Inventor Rt/Explorer Trauma Unit

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K911563 ↗

FDA Product Code

IYB

Device Class

Class I

Regulation

21 CFR Part 892.1770

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• 14X14 Multiformat Spot Filmer, No. 6650.400

  Class II

  FDA 510(k) K881589 Active Cleared 18 Jul 1988

• Floor Mount Tubestand Performer, 6610.101/S-9109

  Class II

  FDA 510(k) K912517 Active Cleared 19 Sep 1991

• Floor Mount Tubestand-Performer-N 6610.102/S-9110

  Class II

  FDA 510(k) K912515 Active Cleared 19 Sep 1991

• Patient Information Manager (Pim)

  Class II

  FDA 510(k) K921986 Active Cleared 16 Oct 1992

• Classic 4-Way Elevating Table

  Class II

  FDA 510(k) K912474 Active Cleared 16 Sep 1991

• Arc Series

  Class II

  FDA 510(k) K954581 Active Cleared 21 Dec 1995

See all devices from Continental X-Ray Corp. →