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..

Clearance details

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

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