# K223464: Leg and Foot Air Wave Pressure Therapy Device

- Pathway: 510(k) (Traditional)
- Applicant: Zhangzhou Easepal Innovation CO, Ltd.
- Decided: Mar 14, 2023 after 117 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K850316 (1985). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K193354: Air Compression Therapy Device, Shenzhen Dongjilian Electronics Co., Ltd. (2020) Summary page 5.

## Indications for use
Leg and Foot Air Wave Pressure Therapy Device EP-1129 is intended for the temporary relief of minor muscle aches and pains and for the temporary increase in circulation to the treated areas in people who are in good health, it can simulate kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K223464
Methodology: https://510kreport.com/methodology