Ultrasound Stimulator— 510(k) K240788

Substantially Equivalent

Jkh Health Co., Ltd.

FDA 510(k) clearance K240788 for Ultrasound Stimulator, Substantially Equivalent on 2025-06-04. Applicant: Jkh Health Co., Ltd.. Device class: 2.

Clearance details

Applicant: Jkh Health Co., Ltd.
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 2024-03-22
Decision date: 2025-06-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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More clearances from Jkh Health Co., Ltd.

K253150 — Cryon-X Cold Compression2025-10-24
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K240011 — Lymphedema Compression2024-02-23
K223541 — Cold/Hot Compression2023-10-27
K211050 — Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-3042022-11-28

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