510(k) · Cleared
ClearedAction Wizard Pediatric Manual Wheelchair
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Invacare Corp. · IOR Wheelchair, Mechanical
Cleared on Dec 15, 1993 after an 85-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 7 later devices descend from it.
- Decided
- Dec 15, 1993
- Review
- 85 days
- Class
- Class I
- Product code
- IOR
- Recalls
- None
- Predicates
- 0
7 later devices descend from it, 1 citing it directly.
- This deviceK934646 Action Wizard Pediatric Manual WheelchairInvacare Corp. · 1993
- Descendant · cites it directly · 6 of its ownK012370 Solara JR. Manual WheelchairInvacare Corp. · 2001 · Recalled
- Descendant · 2 generations on · 2 of its ownK043332 Wheelchair, Model 8500-IICycling and Health Tech. Industry R&D Center · 2004
- Descendant · 2 generations on · 1 of its ownK181090 Invacare® Solara® 3G and Solara® 3G Spree Manual WheelchairsInvacare Corporation · 2018
- Descendant · 2 generations on · 1 of its ownK082274 Haida Model HD11 Manual WheelchairJiangyin East China Medical Technology Co., Ltd. · 2008
- Descendant · 3 generations on · 0 of its ownK200583 Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTLKi Mobility, LLC · 2023
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 7 · See all- K012370Solara JR. Manual WheelchairInvacare Corp. · 2001 · cites it directly6descendants
- K043332Wheelchair, Model 8500-IICycling and Health Tech. Industry R&D Center · 2004 · 2 generations on2descendants
- K181090Invacare® Solara® 3G and Solara® 3G Spree Manual WheelchairsInvacare Corporation · 2018 · 2 generations on1descendant
- K082274Haida Model HD11 Manual WheelchairJiangyin East China Medical Technology Co., Ltd. · 2008 · 2 generations on1descendant
- K200583Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTLKi Mobility, LLC · 2023 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K934646 | Action Wizard Pediatric Manual Wheelchair | Invacare Corp. | 1993 | — |
| +1 | K012370 | Solara JR. Manual Wheelchair | Invacare Corp. | 2001 | 3 |
| +2 | K043332 | Wheelchair, Model 8500-II | Cycling and Health Tech. Industry R&D Center | 2004 | — |
| +2 | K181090 | Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs | Invacare Corporation | 2018 | — |
| +2 | K082274 | Haida Model HD11 Manual Wheelchair | Jiangyin East China Medical Technology Co., Ltd. | 2008 | — |
| +3 | K200583 | Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL | Ki Mobility, LLC | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
| 2004 | 1 | 0 |
| 2008 | 2 | 0 |
| 2010 | 1 | 0 |
| 2018 | 1 | 0 |
| 2023 | 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 IOR? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new IOR device
- #1 K201461 Manual Wheelchair, Model A011score 20.0 · 3 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (7)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K012370 | Solara JR. Manual Wheelchair | 2001 | 6 |
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, K012370 (Invacare Corp., 2001) has gone furthest, with 6 descendants of its own.
How does its category compare?
All IOR devicesIOR Wheelchair, Mechanical: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · IOR
17so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · IOR
91in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · IOR
1in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · IOR
135in 2025
MAUDE reports naming product code IOR, 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 | 5 | 38 | 1 | 36 |
| 2008 | 13 | 32 | 3 | 62 |
| 2009 | 4 | 43 | 2 | 54 |
| 2010 | 12 | 81 | 0 | 69 |
| 2011 | 6 | 58 | 6 | 232 |
| 2012 | 11 | 176 | 3 | 1,238 |
| 2013 | 7 | 233 | 3 | 4,674 |
| 2014 | 7 | 211 | 3 | 5,082 |
| 2015 | 3 | 104 | 0 | 4,472 |
| 2016 | 10 | 135 | 1 | 1,860 |
| 2017 | 7 | 209 | 0 | 49 |
| 2018 | 3 | 203 | 0 | 58 |
| 2019 | 6 | 160 | 0 | 53 |
| 2020 | 2 | — | 0 | 43 |
| 2021 | 2 | — | 1 | 59 |
| 2022 | 4 | 150 | 0 | 37 |
| 2023 | 9 | 61 | 0 | 165 |
| 2024 | 4 | 65 | 0 | 138 |
| 2025 | 7 | 91 | 0 | 135 |
| 2026 | 17 | 103 | 0 | — |
https://510kreport.com/device/K934646 · printed Nov 6, 2026
Cite this page
510(k) Report. “K934646: Action Wizard Pediatric Manual Wheelchair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K934646
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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