# K211283: Compressible Limb and Circulation Therapy System, Model POWER-Q2300

- Pathway: 510(k) (Traditional)
- Applicant: Wonjin Mulsan Co., Ltd.
- Decided: Sep 14, 2021 after 140 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: 8 generations back to K850316 (1985). 19 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182668: Rapid Reboot Compression Therapy System, Rapid Reboot Recovery Products, LLC (2018) Summary page 4.

## Most influential descendants
- K233238: Air Pressure Therapy System (Model:VU-IPC4M) (2024), 0 descendants of its own

## Indications for use
POWER-Q2300 is intended for the temporary relief of minor muscle aches and pains, and for temporary increase in blood circulation to the treated areas in people who are in good health. POWER-Q2300 simulates kneading and stroking of tissues by using an inflatable garment (cuff).

Source page: https://510kreport.com/device/K211283
Methodology: https://510kreport.com/methodology