# K130788: Capella

- Pathway: 510(k) (Traditional)
- Applicant: Future Mobility Healthcare, Inc.
- Decided: Dec 5, 2013 after 258 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: 3 generations back to K941989 (1994). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063736: Fuze Mechanical Wheelchair, Models T20 and T50, Pdg Product Design Group, Inc. (2007) Summary page 2.

## Indications for use
The Future Mobility Healthcare Inc. Capella wheelchair is intended to provide mobility to persons limited to a sitting position.

Source page: https://510kreport.com/device/K130788
Methodology: https://510kreport.com/methodology