# K020472: Biotech Manual Wheelchair B900 Super Light Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Taiwan Armada Enterprise Co., Ltd.
- Decided: Mar 8, 2002 after 24 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
32 later devices descend from it; 2 cite it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K041337: Pro Walker ML-300 Foldable Wheelchair (2004), 30 descendants of its own
- K050290: Lerado, Cosco (2005), 22 descendants of its own
- K050708: Lerado, Avanticare Mechanical Wheelchair, MR-9000 (2005), 20 descendants of its own
- K051482: Jan Mao Wheelchair, Model JMC612-F18EPP (2005), 18 descendants of its own
- K062218: Jan Mao Wheelchair, Models JMC612-FL318EPP and JMC612-FL418EPP (2006), 17 descendants of its own

## Indications for use
The device is intended for medical purposes to provide mobility to person restricted to a sitting position.

Source page: https://510kreport.com/device/K020472
Methodology: https://510kreport.com/methodology