# K231032: AMP by Method Mobility, AMP Plus (or +) by Method Mobility

- Pathway: 510(k) (Traditional)
- Applicant: Method Mobility
- Decided: May 10, 2023 after 29 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K242430: Power-Flex (PFX1214); Power-Flex (PFX1517); Power-Flex (PFX1820) (2024), 0 descendants of its own

## Indications for use
The AMP by Method Mobility is intended to provide enhanced mobility to disabled persons who are capable of operating a powered and manual wheelchair, by providing powered mobility to manual wheelchairs.

Source page: https://510kreport.com/device/K231032
Methodology: https://510kreport.com/methodology