# K241159: Handbike Batec Electric

- Pathway: 510(k) (Traditional)
- Applicant: Batec Mobility, S.L.
- Decided: Mar 7, 2025 after 315 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: 3 generations back to K151199 (2015). 3 ancestors in all.
No later device cites it as a predicate yet.
1 of 4 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222502: Klick (Variants: Power, Race, Monster), Klaxon Mobility GmbH (2022) Summary page 5.

## Indications for use
Batec is not intended for specific clinical use, but as a support to the mobility of active manual wheelchairs' users. It is designed to add auxiliary power to the manual wheelchair, increasing the mobility for the wheelchair's user. Therefore, bearing in mind the operating precautions described in this document, there is no need for professional, technical or aptitude requirements to operate or use a Batec device. Batec devices are intended as add-on devices for wheelchairs, thus the intended user is a person with motor disability who needs of the wheelchair support for movement.

Source page: https://510kreport.com/device/K241159
Methodology: https://510kreport.com/methodology