510(k) Report

510(k) · Cleared

Cleared

Electric Wheelchair

K223393510(k) TraditionalCleared Mar 16, 2023128-day reviewClass II21 CFR 890.3860

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Shanghai Bangbang Robotics Co., Ltd. · ITI Wheelchair, Powered

Cleared on Mar 16, 2023 as substantially equivalent to K213383 (Whill, Inc., 2021) after a 128-day review. Its family tree reaches back 8 generations to 1997. 1 of the 13 devices in its family, counting itself, has a Class I recall. 3 later devices descend from it.

Decided
Mar 16, 2023
Review
128 days
Class
Class II
Product code
ITI
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K960951 (1997). 9 ancestors in all. 3 later devices descend from it, 1 citing it directly. 1 of the 13 devices in this family, counting this one, has a Class I recall.

  1. Root · 8 generations backK960951 Permobil Chairman L/CS 8Permobil AB · 1997
  2. 7 generations backK991658 Permobil Powered Wheelchair 1280Permobil AB · 1999 · Recalled
  3. 6 generations backK041219 ElectroPermobil AB · 2004 · Recalled
  4. 5 generations backK071650 C350 Powered WheelchairPermobil AB · 2007 · Recalled
  5. 4 generations backK103477 Permobil M300 / M400Permobil AB · 2011
  6. 3 generations backK143180 F3Permobil AB · 2015
  7. 2 generations backK153543 WHILL Model MWhill, Inc. · 2016
  8. 1 generation backK213383 WHILL Model C2Whill, Inc. · 2021 · Recalled (Class I)
  9. This deviceK223393 Electric WheelchairShanghai Bangbang Robotics Co., Ltd. · 2023
  10. Descendant · cites it directly · 2 of its ownK231868 Electric Wheelchair (Robooter E40), Model name: BBR-E40-01Shanghai Bangbang Robotics Co., Ltd. · 2023
  11. Descendant · 2 generations on · 0 of its ownK253276 Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair…Shanghai Bangbang Robotics Co., Ltd. · 2026
  12. Descendant · 2 generations on · 0 of its ownK240339 Electric Wheelchair (Robooter E60) (BBR-E60-01); Electric Wheelchair…Shanghai Bangbang Robotics Co., Ltd. · 2024

Class I recalls in this family

Most influential descendants

Showing 3 of 3 · See all
  • K231868Electric Wheelchair (Robooter E40), Model name: BBR-E40-01Shanghai Bangbang Robotics Co., Ltd. · 2023 · cites it directly2descendants
  • K253276Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair (Robooter E80)…Shanghai Bangbang Robotics Co., Ltd. · 2026 · 2 generations on0descendants
  • K240339Electric Wheelchair (Robooter E60) (BBR-E60-01); Electric Wheelchair (Robooter E60)…Shanghai Bangbang Robotics Co., Ltd. · 2024 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K960951Permobil Chairman L/CS 8Permobil AB1997—
−7K991658Permobil Powered Wheelchair 1280Permobil AB19995
−6K041219ElectroPermobil AB20044
−5K071650C350 Powered WheelchairPermobil AB20073
−4K103477Permobil M300 / M400Permobil AB2011—
−3K143180F3Permobil AB2015—
−2K153543WHILL Model MWhill, Inc.2016—
−1K213383WHILL Model C2Whill, Inc.2021Class I
0 (this device)K223393Electric WheelchairShanghai Bangbang Robotics Co., Ltd.2023—
+1K231868Electric Wheelchair (Robooter E40), Model name: BBR-E40-01Shanghai Bangbang Robotics Co., Ltd.2023—
+2K253276Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair (Robooter…Shanghai Bangbang Robotics Co., Ltd.2026—
+2K240339Electric Wheelchair (Robooter E60) (BBR-E60-01); Electric Wheelchair (Robooter…Shanghai Bangbang Robotics Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
202410
202610
FIG. 1 — Lineage of K223393, 1997–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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.

1 device in this family has a Class I recall. 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. #1 K220747 Power Wheelchair (N5515B)score 40.2 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K213383WHILL Model C2
Summary page 4
…Regulation Class: Class 2 Panel: Physical Medicine Product Code: ITI 3. Predicate Device 510(K) number: K213383 Device Name: WHILL Model C2 Manufacturer: Whill, Inc. Common name Wheelchair,…
Whill, Inc.2021Class I

Also cleared against K213383: 2 other devices →

What descends from it? (3)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K231868Electric Wheelchair (Robooter E40), Model name: BBR-E40-01Shanghai Bangbang Robotics Co., Ltd.20232

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K213383WHILL Model C2Whill, Inc. · 2021 · Direct predicate · ◆ on the line of descent in FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 26 years and passes through 3 companies; a new generation was cleared every 3.5 years on median.
  • 4 of the 9 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K231868 (Shanghai Bangbang Robotics Co., Ltd., 2023) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K213383.

How does its category compare?

All ITI devices

ITI Wheelchair, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · ITI

29in 2025

2007: 182008: 92009: 72010: 62011: 42012: 62013: 52014: 52015: 102016: 62017: 42018: 42019: 32020: 62021: 132022: 162023: 82024: 382025: 292026 (partial year): 36
2007high 38 (2024) · low 3 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ITI

90in 2025

2007: 42 days median2008: 49 days median2009: 63 days median2010: 46 days median2011: 101 days median2012: 155 days median2013: 177 days median2014: 213 days median2015: 174 days median2016: 173 days median2017: 159 days median2018: 117 days median2019: 244 days median2020: 278 days median2021: 209 days median2022: 96 days median2023: 128 days median2024: 125 days median2025: 90 days median2026 (partial year): 108 days median
2007high 278 (2020) · low 42 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · ITI

13so far in 2026, the most since 2007

2007: 32008: 32009: 12010: 22012: 12016: 12017: 22021: 32024: 12025: 3, 2 Class I2026 (partial year): 13
2007high 13 (2026) · low 0 (2011)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · ITI

647in 2025

2007: 1232008: 1332009: 1832010: 1572011: 5252012: 2,9192013: 8,7412014: 7,2822015: 4,6852016: 1,5752017: 3012018: 2732019: 2642020: 2052021: 1662022: 1352023: 2232024: 1462025: 647
2007high 8,741 (2013) · low 123 (2007)2025

MAUDE reports naming product code ITI, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200718423123
20089493133
20097631183
20106462157
201141010525
2012615512,919
2013517708,741
2014521307,282
20151017404,685
2016617311,575
201741592301
201841170273
201932440264
202062780205
2021132093166
202216960135
202381280223
2024381251146
202529903 (2)647
20263610813—

What is it indicated for?

The intended use of the Electric Wheelchair (Model: BBR-LY-01-01) is to provide outdoor and indoor mobility to persons limited to a seated position that are capable of operating a powered wheelchair.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K223393: Electric Wheelchair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K223393

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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