Bio Therapy Plus

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K922205 ↗

FDA Product Code

FNM

Device Class

Class II

Regulation

21 CFR Part 880.5550

Advisory Committee

General Hospital

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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• Power Recliner

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• Quickie Rhapsody, Mwd Series II Power Wheelchair

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  FDA 510(k) K062701 Active Cleared 25 Sep 2006

See all devices from Sunrise Medical →