510(k) · Cleared
Recalled · Class II · 2020Quickie, Zippie
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sunrise Medical (Us), LLC · ITI Wheelchair, Powered
Cleared on Dec 18, 2014 as substantially equivalent to K062701 (Sunrise Medical, Inc., 2006) and 1 other predicate after a 107-day review. Its family tree reaches back 1 generation to 2006. 4 later devices descend from it. It has been recalled once.
- Decided
- Dec 18, 2014
- Review
- 107 days
- Class
- Class II
- Product code
- ITI
- Recalls
- 1
- Predicates
- 2
Its longest line of descent runs back 1 generation to K062701 (2006). 2 ancestors in all. 4 later devices descend from it, 4 citing it directly.
- Root · 1 generation backK062701 Quickie Rhapsody, MWD Series II Power WheelchairSunrise Medical, Inc. · 2006
- This deviceK142457 Quickie, ZippieSunrise Medical (Us), LLC · 2014
- Descendant · cites it directly · 0 of its ownK231315 Velox Power ChairVelox Manufacturing, Inc. · 2024
- Descendant · cites it directly · 0 of its ownK213090 Frontier Series Power WheelchairsMagic Mobility · 2021
- Descendant · cites it directly · 0 of its ownK203083 Magic 360 Power WheelchairMagic Mobility · 2021
- Descendant · cites it directly · 0 of its ownK160031 Quickie Pulse (Models 6BC, 6SC, 6CC, 5BC, 5CC, 6MPC) and Zippie…Sunrise Medical (Us), LLC · 2016
Most influential descendants
Showing 4 of 4 · See all- K231315Velox Power ChairVelox Manufacturing, Inc. · 2024 · cites it directly0descendants
- K213090Frontier Series Power WheelchairsMagic Mobility · 2021 · cites it directly0descendants
- K203083Magic 360 Power WheelchairMagic Mobility · 2021 · cites it directly0descendants
- K160031Quickie Pulse (Models 6BC, 6SC, 6CC, 5BC, 5CC, 6MPC) and Zippie ZM-310 (Models BC, SC)Sunrise Medical (Us), LLC · 2016 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K062701 | Quickie Rhapsody, MWD Series II Power Wheelchair | Sunrise Medical, Inc. | 2006 | — |
| 0 (this device) | K142457 | Quickie, Zippie | Sunrise Medical (Us), LLC | 2014 | — |
| +1 | K231315 | Velox Power Chair | Velox Manufacturing, Inc. | 2024 | — |
| +1 | K213090 | Frontier Series Power Wheelchairs | Magic Mobility | 2021 | — |
| +1 | K203083 | Magic 360 Power Wheelchair | Magic Mobility | 2021 | — |
| +1 | K160031 | Quickie Pulse (Models 6BC, 6SC, 6CC, 5BC, 5CC, 6MPC) and Zippie ZM-310 (Models… | Sunrise Medical (Us), LLC | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 1 | 0 |
| 2021 | 2 | 0 |
| 2024 | 1 | 0 |
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 ITI? 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 ITI device
- #1 K220747 Power Wheelchair (N5515B)score 40.2 · 4 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K062701 | Quickie Rhapsody, MWD Series II Power WheelchairSummary page 4…ssification Name: Wheelchair, Powered (21 CFR 890.3860) Regulatory Class: II Product Code: ITI III. PREDICATE DEVICE Quickie Rhapsody, MWD Series II Power Wheelchair, K062701 (Primary Predicate) Quickie Rhythm Power Wheelchair (Controller Change), K083249 (Secondary Predicate) No reference devices wer… | 2006 |
| * | K083249 | Quickie RhythmSummary page 4…uct Code: ITI III. PREDICATE DEVICE Quickie Rhapsody, MWD Series II Power Wheelchair, K062701 (Primary Predicate) Quickie Rhythm Power Wheelchair (Controller Change), K083249 (Secondary Predicate) No reference devices were used in this submission. IV. DEVICE DESCRIPTION The Quickie® and Zippie® p… | 2008 |
What descends from it? (4)
4 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)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Feb 13, 2020 | Class II | Z-1947-2020 | Software Design Change | Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- None of the 2 ancestors has a recall.
- Of its descendants, K231315 (Velox Manufacturing, Inc., 2024) has gone furthest, with 0 descendants of its own.
How does its category compare?
All ITI devicesITI Wheelchair, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · ITI
29in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · ITI
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · ITI
13so far in 2026, the most since 2007
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · ITI
647in 2025
MAUDE reports naming product code ITI, 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 | 18 | 42 | 3 | 123 |
| 2008 | 9 | 49 | 3 | 133 |
| 2009 | 7 | 63 | 1 | 183 |
| 2010 | 6 | 46 | 2 | 157 |
| 2011 | 4 | 101 | 0 | 525 |
| 2012 | 6 | 155 | 1 | 2,919 |
| 2013 | 5 | 177 | 0 | 8,741 |
| 2014 | 5 | 213 | 0 | 7,282 |
| 2015 | 10 | 174 | 0 | 4,685 |
| 2016 | 6 | 173 | 1 | 1,575 |
| 2017 | 4 | 159 | 2 | 301 |
| 2018 | 4 | 117 | 0 | 273 |
| 2019 | 3 | 244 | 0 | 264 |
| 2020 | 6 | 278 | 0 | 205 |
| 2021 | 13 | 209 | 3 | 166 |
| 2022 | 16 | 96 | 0 | 135 |
| 2023 | 8 | 128 | 0 | 223 |
| 2024 | 38 | 125 | 1 | 146 |
| 2025 | 29 | 90 | 3 (2) | 647 |
| 2026 | 36 | 108 | 13 | — |
What is it indicated for?
Quickie® and Zippie® power wheelchairs are battery-operated devices with wheels that are intended for medical purposes to provide mobility to persons restricted to a sitting position. The Zippie® power wheelchairs are specifically for people who are slightly smaller in stature—including children.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K142457 · printed Nov 6, 2026
Cite this page
510(k) Report. “K142457: Quickie, Zippie.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142457
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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