# K201694: Air Compression Therapy Device

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Dongjilian Electronics Co., Ltd.
- Decided: Nov 19, 2020 after 150 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
The Air Compression Therapy Device are indicated for the temporary relief of minor muscle aches and pains and for temporary increase in circulation to the treated areas in people who are in good health. The Air Compression Therapy Device simulates kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K201694
Methodology: https://510kreport.com/methodology