Doctor Tecar Plus, Doctor Tecar Smart— 510(k) K221043

Name: FDA 510(k) clearance K221043
Creator: U.S. Food and Drug Administration
Published: 2023-02-17

Substantially Equivalent

Mectronic Medicale S.R.L.

FDA 510(k) clearance K221043 for Doctor Tecar Plus, Doctor Tecar Smart, Substantially Equivalent on 2023-02-17. Applicant: Mectronic Medicale S.R.L.. Device class: 2.

Clearance details

Applicant: Mectronic Medicale S.R.L.
Product code: Code PBX
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2022-04-08
Decision date: 2023-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grassobbio, IT

Download summary PDF View on FDA.gov ↗

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