# K934560: Wizard  Pediatric Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Snug Seat, Inc.
- Decided: Jan 7, 1994 after 108 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Recalls of this device
- Aug 26, 2013 · Class II · Z-0503-2015: The bolts, which secure the handles, on the Crocodile (size 3) could break, causing the handle to dislodge.

Source page: https://510kreport.com/device/K934560
Methodology: https://510kreport.com/methodology