Fortress 1704FS Four Wheel Scooter

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K922966 ↗

FDA Product Code

INI

FDA applicant

Fortress Scientific , Ltd.

Device Class

Class II

Regulation

21 CFR Part 890.3800

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• 720 Power Base

  Class II

  FDA 510(k) K933864 Active Cleared 28 Mar 1994

• Fortress Buddy Front Wheel Drive Scooter

  Class II

  FDA 510(k) K900042 Active Cleared 12 Jan 1990

• SC930 Seat Controller

  Class II

  FDA 510(k) K933859 Active Cleared 28 Mar 1994

• 770 Power Base

  Class II

  FDA 510(k) K933854 Active Cleared 28 Mar 1994

• Fortress 1700FS Rear Wheel Drive Scooter

  Class II

  FDA 510(k) K922967 Active Cleared 3 Aug 1992

• Fortress Spirit Power Wheelchair

  Class II

  FDA 510(k) K900040 Active Cleared 12 Jan 1990

See all devices from Fortress Scientific, Ltd. →