Air compression Leg Massager (MM0520, MM0521, MM0522)— 510(k) K240373

Name: FDA 510(k) clearance K240373
Creator: U.S. Food and Drug Administration
Published: 2024-09-17

Substantially Equivalent

Zhangzhou Easepal Medical Science and Technology Co., Ltd.

FDA 510(k) clearance K240373 for Air compression Leg Massager (MM0520, MM0521, MM0522), Substantially Equivalent on 2024-09-17. Applicant: Zhangzhou Easepal Medical Science and Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Zhangzhou Easepal Medical Science and Technology Co., Ltd.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2024-02-07
Decision date: 2024-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Zhangzhou, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code IRP

view all

K260944 — ManaCold Compression System2026-08-12
K260529 — Air Compression Massager (HY-1165)2026-07-27
K260948 — Air Compression Massager (EP30B001 I)2026-07-24
K253919 — Cryo And Thermo Therapy System2026-06-10
K252396 — Cryo Sport 2.0 (AVA 501)2026-05-29

More clearances from Zhangzhou Easepal Medical Science and Technology Co., Ltd.

view all

K221800 — Infrared Thermometer (Model: Y20001, Y20002)2022-12-14
K213023 — Blood Pressure Monitor(Model:Y30001)2022-09-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.