# K061273: 7000 Series Lightweight Wheelchair, Models 7160L, 7180L and 7200L

- Pathway: 510(k) (Traditional)
- Applicant: Nova Ortho-Med, Inc.
- Decided: May 23, 2006 after 15 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K881951 (1988). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K881951: Ride-Lite 9000 Series Wheelchair, Invacare Corp. (1988) Summary page 1.

## Most influential descendants
- K131529: Shengguang Manual Wheelchair (2013), 0 descendants of its own

## Indications for use
The intended use of the 7000 Series Lightweight Wheelchair is to provide mobility to adult persons with limited mobility or adult persons limited to a seated position. The target population for the 7000 Series Lightweight Wheelchair is the United States adult population.

Source page: https://510kreport.com/device/K061273
Methodology: https://510kreport.com/methodology