# K090108: Hoveround Teknique FWD MK4 Power Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Hoveround Corp.
- Decided: Mar 19, 2009 after 63 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K122357: Merits Model P322FWD Powered Wheelchair (2013), 0 descendants of its own

## Indications for use
The intended use is to provide mobility to persons limited to a seated position.

Source page: https://510kreport.com/device/K090108
Methodology: https://510kreport.com/methodology