# K151492: Kudu

- Pathway: 510(k) (Traditional)
- Applicant: R82 A/S
- Decided: May 20, 2016 after 352 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K251886: EmpowerRide NAVIGATOR (2026), 0 descendants of its own
- K223533: Little Wave Arc; Little Wave Flip (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K151492
Methodology: https://510kreport.com/methodology