# K952946: Vangator II

- Pathway: 510(k) (Traditional)
- Applicant: Crow River Industries, Inc.
- Decided: Nov 29, 1995 after 156 days
- Product code: ING (Elevator, Wheelchair, Portable)
- Device class: 2
- Regulation: 21 CFR 890.3930
- Recalls of this device: 3 (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 15, 2007 · Not classified · Z-2467-2010: The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.
- Aug 15, 2007 · Not classified · Z-2468-2010: The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.
- Aug 15, 2007 · Not classified · Z-2469-2010: The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.

Source page: https://510kreport.com/device/K952946
Methodology: https://510kreport.com/methodology