# K253064: Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air Pressure Therapy System (VU-IPC4X)

- Pathway: 510(k) (Traditional)
- Applicant: Xiamen Weiyou Intelligent Technology Co., Ltd.
- Decided: Apr 30, 2026 after 220 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: 1 generation back to K243320 (2024). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K243320: Air Pressure Therapy System (VU-IPC04B), Xiamen Weiyou Intelligent Technology Co., Ltd. (2024) Summary page 5.

## Indications for use
Air Pressure Therapy System is intended 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/K253064
Methodology: https://510kreport.com/methodology