# K083017: LEVO C3

- Pathway: 510(k) (Traditional)
- Applicant: Levo AG
- Decided: Oct 24, 2008 after 15 days
- Product code: IPL (Wheelchair, Standup)
- Device class: 2
- Regulation: 21 CFR 890.3900
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K960951 (1997). 9 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030893: Levo Combi, Levo AG (2003) Summary page 1.
- K051387: Levo Comfort II, Levo AG (2005) Summary page 1.
- K071650: C350 Powered Wheelchair, Permobil AB (2007) Summary page 1.

## Most influential descendants
- K172384: Quickie (r) Q700-UP M (2018), 2 descendants of its own
- K233877: XT Series Power Wheelchair  (XT2), XT Series Power Wheelchair  (XT4) (2024), 0 descendants of its own
- K191874: F5 Corpus VS (2019), 0 descendants of its own
- K191376: Modular Power Standing System (2019), 0 descendants of its own

## Indications for use
The LEVO C3 power wheelchair with optional seating and standing position function may be of interest for any individuals who needs a power wheelchair and cannot stand up on their own such as people with spinal cord injury, spina bifida, cerebral palsy, multiple sclerosis, muscular dystrophy, polio, rheumatism, etc..

Source page: https://510kreport.com/device/K083017
Methodology: https://510kreport.com/methodology