# K192618: e-Motion M25

- Pathway: 510(k) (Traditional)
- Applicant: Alber GmbH
- Decided: Nov 2, 2020 after 406 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 K001491 (2000). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 8 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151717: twion, Alber GmbH (2016) Summary page 4.
- K192016: Smoov O10, Alber GmbH (2020). Cleared while this submission was under review Summary page 4.

## Most influential descendants
- K221215: e-motion M25 (2022), 0 descendants of its own

## Indications for use
The e-motion M25 is a Power Assist Wheelchair Conversion Kit and suitable for the manual wheelchair users who are limited in their field of activities because of their physical conditions. The device can expand their field of activities by assisting their wheelchair operating force.

Source page: https://510kreport.com/device/K192618
Methodology: https://510kreport.com/methodology