# K984367: Activx

- Pathway: 510(k) (Traditional)
- Applicant: Adorno Rogers Technology
- Decided: Jan 28, 1999 after 52 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 K890050 (1989). 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)
- K890050: Zippie & Quickie 2HP Wheelchair, Motion Designs, Inc. (1989) Summary page 1.

## Indications for use
Wheelchair mobility, either self-propelled or propelled by an attendant, for the physically impaired.

Source page: https://510kreport.com/device/K984367
Methodology: https://510kreport.com/methodology