# K090856: Journey (or RPSP), Journey Cubic (or Supra or TP02)

- Pathway: 510(k) (Traditional)
- Applicant: Thyssenkrupp Ceteco Srl
- Decided: May 27, 2009 after 58 days
- Product code: ING (Elevator, Wheelchair, Portable)
- Device class: 2
- Regulation: 21 CFR 890.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K893544 (1989). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981486: Stair-Lift, Garaventa (Canada), Ltd. (1998) Summary page 1.

## Most influential descendants
- K102088: Journey Inclined Platform Lift and Supra Curved Incline Platform Lift (2010), 0 descendants of its own

## Indications for use
The Inclined Platform-Lift "JOURNEY" is intended to mechanically transport one person in a wheelchair or in a fold-down seat up and down stairs in a private or public facility either in indoors or outdoors.

Source page: https://510kreport.com/device/K090856
Methodology: https://510kreport.com/methodology