# K983526: Vertical Lift

- Pathway: 510(k) (Traditional)
- Applicant: Barnes,Richardson & Colburn
- Decided: Dec 11, 1998 after 64 days
- Product code: ING (Elevator, Wheelchair, Portable)
- Device class: 2
- Regulation: 21 CFR 890.3930
- Recalls of this device: none
- 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’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Vertical Lift is intended to mechanically transport one person in a wheelchair or in a fold-down seat up and down stairs in a private or public facility either indoors or outdoors.

Source page: https://510kreport.com/device/K983526
Methodology: https://510kreport.com/methodology