510(k) Report

510(k) · Cleared

Cleared

American Bantex MS 4 Mini Scooter

K040754510(k) TraditionalCleared Jul 23, 2004121-day reviewClass II21 CFR 890.3800

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

American Bantex Corp. · INI Vehicle, Motorized 3-Wheeled

Cleared on Jul 23, 2004 as substantially equivalent to K982144 (Mega Motion, Inc., 1999) after a 121-day review. Its family tree reaches back 1 generation to 1999.

Decided
Jul 23, 2004
Review
121 days
Class
Class II
Product code
INI
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K982144 (1999). No later device cites it as a predicate yet.

K982144 · MEGA 4 · Mega Motion, Inc. · 1999199619982000200220042006
K982144 · MEGA 4 · Mega Motion, Inc. · 19990
  1. Root · 1 generation backK982144 MEGA 4Mega Motion, Inc. · 1999
  2. This deviceK040754 American Bantex MS 4 Mini ScooterAmerican Bantex Corp. · 2004
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K982144MEGA 4Mega Motion, Inc.1999—
0 (this device)K040754American Bantex MS 4 Mini ScooterAmerican Bantex Corp.2004—
FIG. 1 — Lineage of K040754, 1999–2004Source: 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.

Planning a device in INI? 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 INI device

  1. #1 K231428 Mobility Scooter (Models: W3431D)score 23.1 · 9 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
*K982144MEGA 4
Summary page 1
…e: 89 INI (890.3800) Vehicle, Motorized 3-Wheeled Legally Marketed Predicate Devices for Substantial Equivalence: *Mega Motion, Inc. - Mega 4 Scooter, K982144 Rationale for SE: The Mega Motion, Mega 4 is a Class 11 device that is intended to provide assistance and help people lead a mor…
Mega Motion, Inc.1999—

Also cleared against K982144: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • Its one ancestor has no recall.
  • 2 other devices also cite its predicate K982144.

How does its category compare?

All INI devices

INI Vehicle, Motorized 3-Wheeled: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · INI

21so far in 2026, the most since 2007

2007: 182008: 72009: 122010: 52011: 52012: 12013: 22014: 12015: 92016: 12017: 52018: 32019: 42020: 12021: 52022: 62023: 92024: 82025: 152026 (partial year): 21
2007high 21 (2026) · low 1 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · INI

111in 2025

2007: 29 days median2008: 28 days median2009: 41 days median2010: 46 days median2011: 130 days median2015: 202 days median2017: 191 days median2018: 266 days median2019: 298 days median2021: 575 days median2022: 159 days median2023: 123 days median2024: 137 days median2025: 111 days median2026 (partial year): 108 days median
2007high 575 (2021) · low 28 (2008)2026

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

Recalls per year · INI

1in 2013

2007: 22010: 32011: 32013: 1
2007high 3 (2010) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · INI

26in 2025

2007: 642008: 292009: 252010: 562011: 702012: 1722013: 4542014: 5672015: 1512016: 762017: 452018: 512019: 252020: 262021: 412022: 412023: 322024: 312025: 26
2007high 567 (2014) · low 25 (2009)2025

MAUDE reports naming product code INI, 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
20071829264
2008728029
20091241025
2010546356
20115130370
20121—0172
20132—1454
20141—0567
201592020151
20161—076
20175191045
20183266051
20194298025
20201—026
20215575041
20226159041
20239123032
20248137031
202515111026
2026211080—

What is it indicated for?

The MS 4 Mini Scooter has been designed to help people who have a difficult time walking. The user must have use of hands and upper-body mobility.

People who have some mobility, but cannot walk for long distances or people that may need crutches to walk will generally purchase this scooter.

The MS 4 Mini Scooter is designed for both indoor and limited outdoor use in clean and dry conditions.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K040754: American Bantex MS 4 Mini Scooter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K040754

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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