# K020539: Tipower Powerdrive and Rimpower X & SX

- Pathway: 510(k) (Traditional)
- Applicant: Tisport
- Decided: Jun 20, 2002 after 121 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
Longest line of descent: 1 generation back to K934232 (1994). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K934232: Commuter (Manual/Power Wheelclhair), Fortress Lite-Style Wheelchairs, Inc. (1994) Summary page 1.

## Indications for use
The intended use of this device (power/manual wheelchair) is the same as the predicate device, the Commuter (K934232). The intended use for the power/manual wheelchair is to provide mobility to physically impaired individuals. These chairs will allow the user to have a battery powered wheelchair or they can disengage the drive mechanism and have a manual wheelchair. The specific medical conditions for which the device is indicated are listed as, but not limited to: Spinal chord injury Stoke/CVA Post Polio Syndrome Spina Bifada Amputee Multiple Sclerosis Arthrogriposis Muscular Dystrophy Lower and upper extremity paralysis

Source page: https://510kreport.com/device/K020539
Methodology: https://510kreport.com/methodology