510(k) Report

510(k) · Cleared

Cleared

Journey (or RPSP), Journey Cubic (or Supra or TP02)

K090856510(k) TraditionalCleared May 27, 200958-day reviewClass II21 CFR 890.3930

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Thyssenkrupp Ceteco Srl · ING Elevator, Wheelchair, Portable

Cleared on May 27, 2009 as substantially equivalent to K981486 (Garaventa (Canada), Ltd., 1998) after a 58-day review. Its family tree reaches back 3 generations to 1989. 1 later device descends from it.

Decided
May 27, 2009
Review
58 days
Class
Class II
Product code
ING
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K893544 (1989). 1 later device descends from it, 1 citing it directly.

  1. Root · 3 generations backK893544 Handi Porch Elevator & Liberty Wheelchair LiftThe Cheney Co. · 1989
  2. 2 generations backK960276 Wheelchair ElevatorServices Industriels Savaria, Inc. · 1996
  3. 1 generation backK981486 Stair-LiftGaraventa (Canada), Ltd. · 1998
  4. This deviceK090856 Journey (or RPSP), Journey Cubic (or Supra or TP02)Thyssenkrupp Ceteco Srl · 2009
  5. Descendant · cites it directly · 0 of its ownK102088 Journey Inclined Platform Lift and Supra Curved Incline Platform LiftThyssenkrupp Ceteco Srl · 2010

Most influential descendants

Showing 1 of 1 · See all
  • K102088Journey Inclined Platform Lift and Supra Curved Incline Platform LiftThyssenkrupp Ceteco Srl · 2010 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K893544Handi Porch Elevator & Liberty Wheelchair LiftThe Cheney Co.1989—
−2K960276Wheelchair ElevatorServices Industriels Savaria, Inc.1996—
−1K981486Stair-LiftGaraventa (Canada), Ltd.1998—
0 (this device)K090856Journey (or RPSP), Journey Cubic (or Supra or TP02)Thyssenkrupp Ceteco Srl2009—
+1K102088Journey Inclined Platform Lift and Supra Curved Incline Platform LiftThyssenkrupp Ceteco Srl2010—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
FIG. 1 — Lineage of K090856, 1989–2010Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in ING? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K981486Stair-Lift
Summary page 1
…Common Device Name: Wheelchair Elevator or Inclined Platform Lift Predicate device: Garaventa Stairlilft GSL Inclined Platform Lift K981486 21CFR 890.3930 Classification code: ING Product description: The JOURNEY c…
Garaventa (Canada), Ltd.1998—

Also cleared against K981486: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K102088Journey Inclined Platform Lift and Supra Curved Incline Platform LiftThyssenkrupp Ceteco Srl20100

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 20 years and passes through 4 companies; a new generation was cleared every 6.8 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K102088 (Thyssenkrupp Ceteco Srl, 2010) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K981486.

How does its category compare?

All ING devices

ING Elevator, Wheelchair, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · ING

1in 2012

2008: 12009: 22010: 12011: 12012: 1
2007high 2 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ING

Too few ING 510(k)s in any year since 2007 to give a median.

Recalls per year · ING

3in 2007

2007: 3
2007high 3 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · ING

4in 2024

2010: 12012: 12017: 22018: 72019: 42020: 72021: 62022: 32023: 22024: 4
2007high 7 (2018) · low 0 (2007)2025

MAUDE reports naming product code ING, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—30
20081—00
20092—00
20101—01
20111—00
20121—01
20130—00
20140—00
20150—00
20160—00
20170—02
20180—07
20190—04
20200—07
20210—06
20220—03
20230—02
20240—04
20250—00
20260—0—

What is it indicated for?

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.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K090856: Journey (or RPSP), Journey Cubic (or Supra or TP02).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K090856

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026