# K240373: Air compression Leg Massager (MM0520, MM0521, MM0522)

- Pathway: 510(k) (Traditional)
- Applicant: Zhangzhou Easepal Medical Science and Technology Co., Ltd.
- Decided: Sep 17, 2024 after 223 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
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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Air compression Leg Massager 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/K240373
Methodology: https://510kreport.com/methodology