510(k) · Cleared
ClearedWheel-O-Vator
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
The National Wheel-O-Vator Co., Inc. · ING Elevator, Wheelchair, Portable
Cleared on Feb 17, 1994 after a 149-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 4 later devices descend from it.
- Decided
- Feb 17, 1994
- Review
- 149 days
- Class
- Class II
- Product code
- ING
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 1 citing it directly.
- This deviceK934553 Wheel-O-VatorThe National Wheel-O-Vator Co., Inc. · 1994
- Descendant · cites it directly · 3 of its ownK960739 V-1504 Vertical Platform LiftBarnes,Richardson & Colburn · 1996
- Descendant · 2 generations on · 1 of its ownK033469 Genesis Vertical Platform LiftGaraventa Accessibility · 2004
- Descendant · 2 generations on · 0 of its ownK113065 RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012
- Descendant · 2 generations on · 0 of its ownK024346 The MultiliftServices Industriels Savaria, Inc. · 2003
Most influential descendants
Showing 4 of 4 · See all- K960739V-1504 Vertical Platform LiftBarnes,Richardson & Colburn · 1996 · cites it directly3descendants
- K033469Genesis Vertical Platform LiftGaraventa Accessibility · 2004 · 2 generations on1descendant
- K113065RL, UL, SL, EL, and Epl Vertical Platform LiftsBella Elevator, LLC · 2012 · 2 generations on0descendants
- K024346The MultiliftServices Industriels Savaria, Inc. · 2003 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K934553 | Wheel-O-Vator | The National Wheel-O-Vator Co., Inc. | 1994 | — |
| +1 | K960739 | V-1504 Vertical Platform Lift | Barnes,Richardson & Colburn | 1996 | — |
| +2 | K033469 | Genesis Vertical Platform Lift | Garaventa Accessibility | 2004 | — |
| +2 | K113065 | RL, UL, SL, EL, and Epl Vertical Platform Lifts | Bella Elevator, LLC | 2012 | — |
| +2 | K024346 | The Multilift | Services Industriels Savaria, Inc. | 2003 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
| 2012 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), 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
What was it cleared against?
FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K960739 | V-1504 Vertical Platform Lift | 1996 | 3 |
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?
- Of its descendants, K960739 (Barnes,Richardson & Colburn, 1996) has gone furthest, with 3 descendants of its own.
How does its category compare?
All ING devicesING Elevator, Wheelchair, Portable: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · ING
1in 2012
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
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · ING
4in 2024
MAUDE reports naming product code ING, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 3 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 2 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 1 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 1 | — | 0 | 1 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 2 |
| 2018 | 0 | — | 0 | 7 |
| 2019 | 0 | — | 0 | 4 |
| 2020 | 0 | — | 0 | 7 |
| 2021 | 0 | — | 0 | 6 |
| 2022 | 0 | — | 0 | 3 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 4 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K934553 · printed Nov 4, 2026
Cite this page
510(k) Report. “K934553: Wheel-O-Vator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K934553
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026