Power Drive Wheelchair-Various

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K851381 ↗

FDA Product Code

ITI

Device Class

Class II

Regulation

21 CFR Part 890.3860

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Runaround

  Class II

  FDA 510(k) K862405 Active Cleared 15 Jul 1986

• Power Drive Wheelchair

  Class II

  FDA 510(k) K853649 Active Cleared 5 Nov 1985

• Specialty Controls Interface

  Class II

  FDA 510(k) K913645 Active Cleared 17 Dec 1991

• Modular Power Base

  Class II

  FDA 510(k) K854051 Active Cleared 27 Dec 1985

• Record

  Class I

  FDA 510(k) K940303 Active Cleared 17 Feb 1994

• S.P.F. Premier 2 Wheelchair

  Class I

  FDA 510(k) K904152 Active Cleared 19 Sep 1990

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