# K140706: Levo Max

- Pathway: 510(k) (Traditional)
- Applicant: Levo AG
- Decided: Jan 21, 2015 after 306 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: 5 generations back to K960951 (1997). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123290: M300 & M400, Permobil AB (2013) Summary page 4.

## Indications for use
The LEVO MAX power wheelchair is intended to provide indoor and outdoor mobility to persons limited to a sitting position, that are capable of operating a powered wheelchair.

Source page: https://510kreport.com/device/K140706
Methodology: https://510kreport.com/methodology