# K243320: Air Pressure Therapy System (VU-IPC04B)

- Pathway: 510(k) (Special)
- Applicant: Xiamen Weiyou Intelligent Technology Co., Ltd.
- Decided: Nov 18, 2024 after 26 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices 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.

## Most influential descendants
- K253064: Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air Pressure Therapy System (VU-IPC4X) (2026), 0 descendants of its own
- K242615: Intermittent pressure compression system (Compression Pump PT1005A; Leg Compression Cuffs; L-1001S, L-1001L, L-1001XL, L-1001XXL, L-1001XXXL) (2025), 0 descendants of its own

## Indications for use
The 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/K243320
Methodology: https://510kreport.com/methodology