Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500— 510(k) K222260

Name: FDA 510(k) clearance K222260
Creator: U.S. Food and Drug Administration
Published: 2023-03-28

Substantially Equivalent

Capenergy Medical S.L.

FDA 510(k) clearance K222260 for Capenergy C Equipment RF System - C25, C50, C100, C200, C300, C400, C500, Substantially Equivalent on 2023-03-28. Applicant: Capenergy Medical S.L.. Device class: 2.

Clearance details

Applicant: Capenergy Medical S.L.
Product code: Code PBX
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2022-07-28
Decision date: 2023-03-28
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Sant Joan Despi, Barcelona, ES

Download summary PDF View on FDA.gov ↗

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