# K233238: Air Pressure Therapy System (Model:VU-IPC4M)

- Pathway: 510(k) (Traditional)
- Applicant: Xiamen Weiyou Intelligent Technology Co., Ltd.
- Decided: Jun 14, 2024 after 260 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). 24 ancestors in all.
No later device cites it as a predicate yet.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211745: RecoveryAir PRO, Theragun, Inc. (2021) Summary page 6.
- K211283: Compressible Limb and Circulation Therapy System, Model POWER-Q2300, Wonjin Mulsan Co., Ltd. (2021) Summary page 6.
- K210913: V12 PRO, Slk Medical GmbH (2021) Summary page 6.

## Indications for use
Air Pressure Therapy System (Model:VU-IPC4M) is intended for home to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas in people who are in good health.

Source page: https://510kreport.com/device/K233238
Methodology: https://510kreport.com/methodology