# K000796: Magic Mobility 4 X 4 Wheelchair

- Pathway: 510(k) (Abbreviated)
- Applicant: Vestil Manufacturing Corp.
- Decided: Aug 11, 2000 after 151 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
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K090350: Extreme 4X4-X8 Power Wheelchair (2009), 3 descendants of its own
- K211574: Extreme X8 (2021), 1 descendant of its own
- K233877: XT Series Power Wheelchair  (XT2), XT Series Power Wheelchair  (XT4) (2024), 0 descendants of its own
- K152672: Cajun Commando 4x4 (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K000796
Methodology: https://510kreport.com/methodology