# K984391: The Liberator

- Pathway: 510(k) (Abbreviated)
- Applicant: Liberator Wheelchairs, Inc.
- Decided: Sep 3, 1999 after 269 days
- Product code: IPL (Wheelchair, Standup)
- Device class: 2
- Regulation: 21 CFR 890.3900
- 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 Liberator wheelchair will be used for paraplegics to afford them the opportunity to be in a standing position while moving around in the wheelchair. It also provides the opportunity for better circulation by allowing the user to change positions as often as the user wants which reduces the risk of skin excoriation.

Source page: https://510kreport.com/device/K984391
Methodology: https://510kreport.com/methodology