# K143014: F5

- Pathway: 510(k) (Traditional)
- Applicant: Permobil AB
- Decided: Mar 25, 2015 after 156 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.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K103477: Permobil M300 / M400, Permobil AB (2011) Summary page 4.

## Most influential descendants
- K191874: F5 Corpus VS (2019), 0 descendants of its own

## Indications for use
The intended use of the F5 powered wheelchair is to provide indoor and outdoor mobility to persons limited to a seating position that are capable of operating a powered wheelchair.

Source page: https://510kreport.com/device/K143014
Methodology: https://510kreport.com/methodology