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FDA 510(k)

Air compression leg massager

K-Number: K240981 · 2024-08-02

Decision Date2024-08-02
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air compression leg massager is a medical device manufactured by Huizhou Xinyi Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-08-02 under approval number K240981. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Air compression leg massager?

Air compression leg massager is a medical device that received FDA 510(k) clearance on 2024-08-02. It is manufactured by Huizhou Xinyi Technology Co., Ltd.. The 510(k) number is K240981.

When was Air compression leg massager approved by the FDA?

Air compression leg massager received FDA 510(k) clearance on 2024-08-02, under approval number K240981.

What company makes Air compression leg massager?

Air compression leg massager is manufactured by Huizhou Xinyi Technology Co., Ltd..

What is the FDA product code for Air compression leg massager?

The FDA product code for Air compression leg massager is IRP.

Other Devices by Huizhou Xinyi Technology Co., Ltd.

Related Devices (Code: IRP)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.