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FDA 510(k)

Air compression Leg Massager (MM0520, MM0521, MM0522)

K-Number: K240373 · 2024-09-17

ApplicantZhangzhou Easepal Medical Science and Technology Co., Ltd.
Decision Date2024-09-17
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air compression Leg Massager (MM0520, MM0521, MM0522) is a medical device manufactured by Zhangzhou Easepal Medical Science and Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-09-17 under approval number K240373. 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 (MM0520, MM0521, MM0522)?

Air compression Leg Massager (MM0520, MM0521, MM0522) is a medical device that received FDA 510(k) clearance on 2024-09-17. It is manufactured by Zhangzhou Easepal Medical Science and Technology Co., Ltd.. The 510(k) number is K240373.

When was Air compression Leg Massager (MM0520, MM0521, MM0522) approved by the FDA?

Air compression Leg Massager (MM0520, MM0521, MM0522) received FDA 510(k) clearance on 2024-09-17, under approval number K240373.

What company makes Air compression Leg Massager (MM0520, MM0521, MM0522)?

Air compression Leg Massager (MM0520, MM0521, MM0522) is manufactured by Zhangzhou Easepal Medical Science and Technology Co., Ltd..

What is the FDA product code for Air compression Leg Massager (MM0520, MM0521, MM0522)?

The FDA product code for Air compression Leg Massager (MM0520, MM0521, MM0522) is IRP.

Other Devices by Zhangzhou Easepal Medical Science and Technology Co., Ltd.

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Official Source

View on FDA Database →

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

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