# K990555: Tisport X and Tisport XC

- Pathway: 510(k) (Traditional)
- Applicant: Tisport
- Decided: Mar 22, 1999 after 28 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- 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 K890050 (1989). 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)
- K890050: Zippie & Quickie 2HP Wheelchair, Motion Designs, Inc. (1989) Summary page 1.

## Indications for use
The intended use of this device (folding manual wheelchair) is the same as the predicate device, Sunrise's Quickie 2HP folding wheelchair (K890050). It is intended to provide mobility to physically impaired individuals. The manual wheelchair is intended for on-going “everyday” use. 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/K990555
Methodology: https://510kreport.com/methodology