# K092225: Amypower All Track Series Power Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Amylior, Inc.
- Decided: Oct 9, 2009 after 78 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K900565 (1990). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023589: Storm TDX Power Wheelchair, Invacare Corp. (2002) Summary page 1.
- K940051: Action Storm Power Wheelchair, Invacare Corp. (1994) Summary page 1.

## Most influential descendants
- K193599: BOUNDER 300 Power Wheelchair, BOUNDER Plus 300 Power Wheelchair, BOUNDER 450 Power Wheelchair, BIG BOUNDER 600 Power Wheelchair, BIG BOUNDER 1000 Power Wheelchair (2020), 0 descendants of its own

## Indications for use
The AMYPOWER ALLTRACK power wheelchairs intended use is to provide mobility to persons limited to a seating position, that have the capability of operating a powered wheelchair. The AMYPOWER ALLTRACK power wheelchair empowers physically challenged individuals by providing a means of mobility.

Source page: https://510kreport.com/device/K092225
Methodology: https://510kreport.com/methodology