510(k) · Cleared
ClearedElectric Wheelchair [Models: JRWD6010/JRWD6012]
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Jerry Medical Instrument (Shanghai) Co., Ltd. · ITI Wheelchair, Powered
Cleared on Jul 13, 2021 as substantially equivalent to K170787 (Nanjing Jin Bai HE Medical Apparatus Co., Ltd., 2017) after a 652-day review. Its family tree reaches back 1 generation to 2017. 2 later devices descend from it.
- Decided
- Jul 13, 2021
- Review
- 652 days
- Class
- Class II
- Product code
- ITI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K170787 (2017). 2 later devices descend from it, 2 citing it directly.
- Root · 1 generation backK170787 Powered Wheelchair DYW30A (D09)Nanjing Jin Bai HE Medical Apparatus Co., Ltd. · 2017
- This deviceK192739 Electric Wheelchair [Models: JRWD6010/JRWD6012]Jerry Medical Instrument (Shanghai) Co., Ltd. · 2021
- Descendant · cites it directly · 0 of its ownK221799 Electric Wheelchair, Model: 9000NSilver Fox Corporation Limited · 2022
- Descendant · cites it directly · 0 of its ownK220827 Electric WheelchairFoshan Dahao Medical Technology Co., Ltd. · 2022
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K170787 | Powered Wheelchair DYW30A (D09) | Nanjing Jin Bai HE Medical Apparatus Co., Ltd. | 2017 | — |
| 0 (this device) | K192739 | Electric Wheelchair [Models: JRWD6010/JRWD6012] | Jerry Medical Instrument (Shanghai) Co., Ltd. | 2021 | — |
| +1 | K221799 | Electric Wheelchair, Model: 9000N | Silver Fox Corporation Limited | 2022 | — |
| +1 | K220827 | Electric Wheelchair | Foshan Dahao Medical Technology Co., Ltd. | 2022 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2022 | 2 | 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K170787 | Powered Wheelchair DYW30A (D09)Summary page 5…l Apparatus Co., Ltd. Device: Powered Wheelchair DYW30A(D09) 1 of page 10 510(k) Summary 510(k) number: K170787 5.0 Indication for Use Statement The device is a motor-driven, and indoor transportation vehicle with the intended use to provi… | 2017 |
| † | K202482 | Y207 Electric Wheelchair | 2021 |
What descends from it? (2)
2 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?
How does its category compare?
All ITI devicesITI Wheelchair, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, 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?
The device is a motor-driven, and indoor transportation vehicle with the intended use to provide mobility to a disabled or an elderly person limited to a seated position.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K192739 · printed Nov 6, 2026
Cite this page
510(k) Report. “K192739: Electric Wheelchair [Models: JRWD6010/JRWD6012].” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192739
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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