# K080270: Manual Rigid Mobility Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Freedom Designs, Inc.
- Decided: Apr 16, 2008 after 75 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
No predicates in its family tree.
2 later devices descend from it; 2 cite 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)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K151893: P.R.O. CG Manual Wheelchair (2015), 0 descendants of its own
- K111636: Rehab TNT, Rehab Ram, Rehab Mac, Rehab Kidster, Bariatric Rehab TNT and Rehab Ram (2012), 0 descendants of its own

## Indications for use
This wheelchair is designed as a transport base for pediatric and adult clients.

Source page: https://510kreport.com/device/K080270
Methodology: https://510kreport.com/methodology