CAPENERGY - C100, C200, C300, C400, C50— 510(k) K191202

Name: FDA 510(k) clearance K191202
Creator: U.S. Food and Drug Administration
Published: 2020-02-11

Substantially Equivalent

Capenergy Medical S.L.

FDA 510(k) clearance K191202 for CAPENERGY - C100, C200, C300, C400, C50, Substantially Equivalent on 2020-02-11. 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: 2019-05-06
Decision date: 2020-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sant Joan Despi, Barcelona, ES

Download summary PDF View on FDA.gov ↗

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