# K992619: Amigo Model 680000 (Amigo Excite F 350)

- Pathway: 510(k) (Traditional)
- Applicant: Amigo Mobility Intl., Inc.
- Decided: Oct 25, 1999 after 82 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K077247: AMIGO MODEL 620000 Excite F350. Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Indications for use
The subject device and the predicate device intended use is personal transportation for walking impaired individuals.

Source page: https://510kreport.com/device/K992619
Methodology: https://510kreport.com/methodology