Zionic Pro Max (Radiofrequency)— 510(k) K243716

Name: FDA 510(k) clearance K243716
Creator: U.S. Food and Drug Administration
Published: 2025-05-28

Substantially Equivalent

Termosalud S.L.

FDA 510(k) clearance K243716 for Zionic Pro Max (Radiofrequency), Substantially Equivalent on 2025-05-28. Applicant: Termosalud S.L.. Device class: 2.

Clearance details

Applicant: Termosalud S.L.
Product code: Code PBX
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2024-12-02
Decision date: 2025-05-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gijon, ES

Download summary PDF View on FDA.gov ↗

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