# K902438: RX Rocker Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: The RX Rocker Corp.
- Decided: Jun 19, 1990 after 18 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K052548: Urok Rocking Wheelchair, Model 700-4XX (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K902438
Methodology: https://510kreport.com/methodology