Golden Spyder, Model Gs-300

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K041341 ↗

FDA Product Code

ITI

Device Class

Class II

Regulation

21 CFR Part 890.3860

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Golden Hawk

  Class II

  FDA 510(k) K971050 Active Cleared 1 Aug 1997

• Companion Model 221, 321, 421

  Class II

  FDA 510(k) K012258 Active Cleared 3 Dec 2001

• Golden Eagle

  Class II

  FDA 510(k) K971043 Active Cleared 1 Aug 1997

• Alante, Battery Operated Power Wheelchair

  Class II

  FDA 510(k) K011153 Active Cleared 29 May 2001

• Buzzaround, Vehicle, Motorized 3-Wheeled

  Class II

  FDA 510(k) K041025 Active Cleared 3 May 2004

• Golden Power Lift Chair

  Class II

  FDA 510(k) K880800 Active Cleared 14 Mar 1988

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