# K223533: Little Wave Arc; Little Wave Flip

- Pathway: 510(k) (Traditional)
- Applicant: Ki Mobility, LLC
- Decided: Aug 31, 2023 after 281 days
- Product code: LBE (Stroller, Adaptive)
- 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
Longest line of descent: 1 generation back to K151492 (2016). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151492: Kudu, R82 A/S (2016) Summary page 4.

## Indications for use
The Ki Mobility Little Wave Arc and Little Wave Flip manual wheelchairs are intended to provide mobility to pediatrics limited to a seating position.

Source page: https://510kreport.com/device/K223533
Methodology: https://510kreport.com/methodology