XOD Diathermia Radiofrequency Device— 510(k) K242175

Substantially Equivalent

Xod, Inc.

FDA 510(k) clearance K242175 for XOD Diathermia Radiofrequency Device, Substantially Equivalent on 2025-02-27. Applicant: Xod, Inc.. Device class: 2.

Clearance details

Applicant: Xod, Inc.
Product code: Code PBX
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2024-07-24
Decision date: 2025-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Philadelphia, PA, US

Download summary PDF View on FDA.gov ↗

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