# K023005: Aquilla Modular Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Haywood Vocational Opportunities
- Decided: Oct 18, 2002 after 39 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 K974820 (1998). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K974820: Breezy Series, Sunrise Medical, Inc. (1998) Summary page 2.

## Indications for use
The Aquilla Modular Wheelchair is intended to provide mobility for occupants who are unable to walk or have difficulty in walking without assistance.

Source page: https://510kreport.com/device/K023005
Methodology: https://510kreport.com/methodology