Journey (or RPSP), Journey Cubic (or Supra or TP02)
FDA 510(k) K090856 · Thyssenkrupp Ceteco Srl
510(k) numberK090856
Submission
- Device name
- Journey (or RPSP), Journey Cubic (or Supra or TP02)
- Applicant
- Thyssenkrupp Ceteco Srl
Pisa, IT - Received
- March 30, 2009
- Decision date
- May 27, 2009
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- ING – Elevator, Wheelchair, Portable
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.3930
- Specialty
- Physical Medicine
A motorized lift device that is not permanently mounted in one location and that is intended for medical purposes to provide a means to move a person with impaired mobility, with or without a wheelchair, from one level to another (e.g., portable platform lifts, attendant-operated stair climbing devices for wheelchairs).
Other 510(k)s with product code ING
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K113065 | RL, Ul, SL, El, and Epl Vertical Platform LiftsING · Traditional | Bella Elevator, LLC | 02/22/2012SE |
| K110495 | Liftkar PTING · Traditional | Sano Transportgerate GmbH | 05/20/2011SE |
| K102088 | Journey Inclined Platform Lift and Supra Curved Incline Platform LiftING · Special | Thyssenkrupp Ceteco Srl | 10/20/2010SE |
| K091881 | Rpl/Cpl Vertical Platform LiftsING · Traditional | Harmar Summit, LLC | 07/01/2009SE |
| K073513 | Merits E700 Porce LiftING · Abbreviated | Merits Health Products Co., Ltd. | 01/14/2008SE |
| K061514 | Bruno Vertical Platform Lift, Model VPL-3100ING · Traditional | Bruno Independent Living Aids, Inc. | 07/13/2006SE |
| K033469 | Genesis Vertical Platform LiftING · Abbreviated | Garaventa Accessibility | 01/07/2004SE |
| K024346 | The MultiliftING · Traditional | Services Industriels Savaria, Inc. | 03/04/2003SE |
| K020933 | Garaventa Super-Trac TRE-52ING · Special | Garaventa Accessibility | 04/04/2002SE |
| K983526 | Vertical LiftING · Traditional | Barnes,Richardson & Colburn | 12/11/1998SE |
More from Barnes,Richardson & Colburn
| 510(k) | Device | Decision |
|---|---|---|
| K102088 | Journey Inclined Platform Lift and Supra Curved Incline Platform LiftING · Special | 10/20/2010SE |
Questions and answers
When was Journey (or RPSP), Journey Cubic (or Supra or TP02) cleared by the FDA?
Journey (or RPSP), Journey Cubic (or Supra or TP02) (K090856) received a 510(k) decision of Substantially Equivalent on May 27, 2009, 58 days after the submission was received.
What is the product code of K090856?
The FDA product code is ING – Elevator, Wheelchair, Portable, a Class II (moderate risk) device regulated under 21 CFR 890.3930.