IPL Treatment Device (MDSQMC-01)— 510(k) K243123

Name: FDA 510(k) clearance K243123
Creator: U.S. Food and Drug Administration
Published: 2025-07-03

Substantially Equivalent

Medusa (Guangxi)Medical Devices Co., Ltd.

FDA 510(k) clearance K243123 for IPL Treatment Device (MDSQMC-01), Substantially Equivalent on 2025-07-03. Applicant: Medusa (Guangxi)Medical Devices Co., Ltd.. Device class: 2.

Clearance details

Applicant: Medusa (Guangxi)Medical Devices Co., Ltd.
Product code: Code ONF
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2024-09-30
Decision date: 2025-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yulin, CN

Download summary PDF View on FDA.gov ↗

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