# K192216: Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corporation
- Decided: Jan 2, 2020 after 140 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K900565 (1990). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170507: Invacare® TDX® SP2 Power Wheelchair; TDXSP2 TDX SP2 with LiNX Electronics, TDXSP2-CG TDX SP2 Base for Single Act. System w/ Ultra Low Maxx, TDXSP2-MCG TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx, Invacare Corporation (2017) Summary page 4.

## Most influential descendants
- K202379: Invacare AVIVA Storm RX Power Chair (2021), 0 descendants of its own

## Recalls of this device
- Nov 12, 2021 · Class II · Z-0446-2022: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect decele

## Indications for use
The Invacare® AVIVA FX Power Wheelchair is indicated to provide mobility and positioning to persons limited to a sitting position.

Source page: https://510kreport.com/device/K192216
Methodology: https://510kreport.com/methodology