Air compression Leg Massager (MM0520, MM0521, MM0522)
K-Number: K240373 · 2024-09-17
Device Summary
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. The listed applicant is Zhangzhou Easepal Medical Science and Technology Co., Ltd.. The 510(k) number is K240373.
When did Air compression Leg Massager (MM0520, MM0521, MM0522) receive FDA 510(k) clearance?
Air compression Leg Massager (MM0520, MM0521, MM0522) received FDA 510(k) clearance on 2024-09-17, under 510(k) number K240373.
Who is the listed applicant for Air compression Leg Massager (MM0520, MM0521, MM0522)?
The FDA 510(k) record lists Zhangzhou Easepal Medical Science and Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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 records listing Zhangzhou Easepal Medical Science and Technology Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IRP)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.