# K192466: Air Compression Therapy System

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Lifotronic Technology Co., Ltd.
- Decided: Jun 22, 2020 after 287 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: 5 generations back to K914774 (1992). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102320: Compressible Limb and Circulation Therapy System Model LX7(V7), Daesung Maref Co., Ltd. (2011) Summary page 4.

## Indications for use
Airpro-690 is intended for use by medical professionals and patients at home, who are under medical supervision, in treating many conditions, such as Primary lymphedema, Edema following trauma and sport injuries, Post immobilization edema, Venous insufficiencies, Lymphedema.

Source page: https://510kreport.com/device/K192466
Methodology: https://510kreport.com/methodology