510(k) · Cleared
ClearedQuickie Wheelchairs
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Motion Designs, Inc. · IOR Wheelchair, Mechanical
Cleared on May 2, 1985 after an 80-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 13 later devices descend from it.
- Decided
- May 2, 1985
- Review
- 80 days
- Class
- Class I
- Product code
- IOR
- Recalls
- None
- Predicates
- 0
13 later devices descend from it, 4 citing it directly.
- This deviceK850536 Quickie WheelchairsMotion Designs, Inc. · 1985
- Descendant · cites it directly · 4 of its ownK120628 HELIOMotion Composites · 2012
- Descendant · cites it directly · 4 of its ownK062660 CatalysyKi Mobility, LLC · 2006
- Descendant · 2 generations on · 3 of its ownK161425 APEX Manual WheelchairMotion Composites · 2016
- Descendant · 2 generations on · 3 of its ownK113713 Gen_2 Mechanical WheelchairFree Wheelchair Mission · 2012
- Descendant · 3 generations on · 2 of its ownK141691 GEN_3Free Wheelchair Mission · 2014
Showing 5 of 13 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 13 · See all- K120628HELIOMotion Composites · 2012 · cites it directly4descendants
- K062660CatalysyKi Mobility, LLC · 2006 · cites it directly4descendants
- K161425APEX Manual WheelchairMotion Composites · 2016 · 2 generations on3descendants
- K113713Gen_2 Mechanical WheelchairFree Wheelchair Mission · 2012 · 2 generations on3descendants
- K141691GEN_3Free Wheelchair Mission · 2014 · 3 generations on2descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K850536 | Quickie Wheelchairs | Motion Designs, Inc. | 1985 | — |
| +1 | K120628 | HELIO | Motion Composites | 2012 | — |
| +1 | K062660 | Catalysy | Ki Mobility, LLC | 2006 | — |
| +2 | K161425 | APEX Manual Wheelchair | Motion Composites | 2016 | — |
| +2 | K113713 | Gen_2 Mechanical Wheelchair | Free Wheelchair Mission | 2012 | — |
| +3 | K141691 | GEN_3 | Free Wheelchair Mission | 2014 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 1 | 0 |
| 2006 | 1 | 0 |
| 2008 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 2 | 0 |
| 2014 | 1 | 0 |
| 2016 | 1 | 0 |
| 2017 | 1 | 0 |
| 2025 | 1 | 0 |
| 2026 | 3 | 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? (13)
See all 134 later devices cite it directly; ranked here by how many devices descend from each in turn.
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, K120628 (Motion Composites, 2012) has gone furthest, with 4 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/K850536 · printed Nov 3, 2026
Cite this page
510(k) Report. “K850536: Quickie Wheelchairs.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K850536
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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