# K011744: HP-5, Battery Operated, Rear Wheel Drive, Power Wheelchair

- Pathway: 510(k) (Abbreviated)
- Applicant: Transworld Mobility Distribution, LLC
- Decided: Aug 24, 2001 after 80 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- 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 intended use of the HP-5 is to provide mobility to adults limited to a sitting position that have the capacity to operate a simple hand control and also allow this chair to fold for easy transportation.

Source page: https://510kreport.com/device/K011744
Methodology: https://510kreport.com/methodology