# K982145: MEGA 3

- Pathway: 510(k) (Traditional)
- Applicant: Mega Motion, Inc.
- Decided: Apr 14, 1999 after 301 days
- Product code: INI (Vehicle, Motorized 3-Wheeled)
- Device class: 2
- Regulation: 21 CFR 890.3800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Pace Saver Plus III Premier: named in the summary without a submission number

## Most influential descendants
- K060697: Travel Pal (MM-111B) /Mega Motion (2006), 1 descendant of its own
- K080288: Travel Pal Four Wheel Scooter, Model MM114 (2008), 0 descendants of its own
- K042104: American Bantex, Model MS 3 (2004), 0 descendants of its own

## Indications for use
The Mega 3 scooter is intended to help the user achieve a more independent lifestyle by increasing their personal mobility. The Mega 3 scooter is intended for use by people who due to medical reasons, accident, or injury do not have adequate mobility to lead the active lifestyle they want. It is also intended for any person who would simply rather ride a scooter than walk.

Source page: https://510kreport.com/device/K982145
Methodology: https://510kreport.com/methodology