Air Pressure Therapy System (VU-IPC04B)

FDA 510(k) K243320 · Xiamen Weiyou Intelligent Technology Co., Ltd.

Substantially Equivalent

510(k) numberK243320

Submission

Device name
Air Pressure Therapy System (VU-IPC04B)
Applicant
Xiamen Weiyou Intelligent Technology Co., Ltd.
Xiamen, CN
Received
October 23, 2024
Decision date
November 18, 2024
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
IRP – Massager, Powered Inflatable Tube
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5650
Specialty
Physical Medicine

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K254200Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1…IRP · Traditional Wenzhou Lingfeng Electronic Technology Co., Ltd.05/05/2026SE
K253064Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air…IRP · Traditional Xiamen Weiyou Intelligent Technology Co., Ltd.04/30/2026SE
K252386Hot and Cold Compression System (A02-C-032)IRP · Traditional Chengdu Cryo-Push Medical Technology Co.,Ltd04/03/2026SE
K253076Cryopush Cold Compression Device (A02-P-001)IRP · Traditional Chengdu Cryo-Push Medical Technology Co.,Ltd04/02/2026SE
K251622Hand Massager (SM004D)IRP · Traditional Ningbo Zhenhai Yihao Electronic Technology Co.…01/28/2026SE

More from Ningbo Zhenhai Yihao Electronic Technology Co., Ltd.

510(k)DeviceDecision
K253919Cryo And Thermo Therapy SystemIRP · Traditional 06/10/2026SE
K253064Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air…IRP · Traditional 04/30/2026SE
K243791Air Pressure Therapy SystemIRP · Special 01/13/2025SE
K233238Air Pressure Therapy System (Model:VU-IPC4M)IRP · Traditional 06/14/2024SE
K201935Air Pressure Therapy SystemIRP · Traditional 06/22/2021SE
K210967Air Pressure Therapy System: VU-IPC06IRP · Traditional 05/11/2021SE

Questions and answers

When was Air Pressure Therapy System (VU-IPC04B) cleared by the FDA?

Air Pressure Therapy System (VU-IPC04B) (K243320) received a 510(k) decision of Substantially Equivalent on November 18, 2024, 26 days after the submission was received.

What is the product code of K243320?

The FDA product code is IRP – Massager, Powered Inflatable Tube, a Class II (moderate risk) device regulated under 21 CFR 890.5650.