# K020639: Tipower TR Rimpower and Tipower Tra Rimpower

- Pathway: 510(k) (Traditional)
- Applicant: Tisport
- Decided: Jun 20, 2002 after 113 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 powerlmanual 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/K020639
Methodology: https://510kreport.com/methodology