Quickie G Series, Model G-424

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K983677 ↗

FDA Product Code

ITI

Device Class

Class II

Regulation

21 CFR Part 890.3860

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

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• Quickie Interchange Fwd W/Lift Power Wheelchair

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• Quickie Freestyle Power Wheelchair, Model G-424

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