# K934646: Action Wizard Pediatric Manual Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corp.
- Decided: Dec 15, 1993 after 85 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.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K012370: Solara JR. Manual Wheelchair (2001), 6 descendants of its own
- K043332: Wheelchair, Model 8500-II (2004), 2 descendants of its own
- K181090: Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs (2018), 1 descendant of its own
- K082274: Haida Model HD11 Manual Wheelchair (2008), 1 descendant of its own
- K200583: Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K934646
Methodology: https://510kreport.com/methodology