# K940051: Action Storm Power Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corp.
- Decided: Mar 28, 1994 after 82 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 3 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K993413: Storm Series, Power 9000 Series and Power Tiger with Gyroscope Control (1999), 2 descendants of its own
- K092225: Amypower All Track Series Power Wheelchair (2009), 1 descendant of its own
- K963808: Choice Powered Wheelchair (1997), 1 descendant of its own
- 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
- K042699: Ability Power Gurney (2005), 0 descendants of its own

## Recalls of this device
- Jan 15, 2015 · Class II · Z-1139-2015: If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight may cause the headrest knob or clamp bracket to pinch, damage or cut the wire. Smoking, sp

Source page: https://510kreport.com/device/K940051
Methodology: https://510kreport.com/methodology