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FDA 510(k)

XOD Diathermia Radiofrequency Device

K-Number: K242175 · 2025-02-27

ApplicantXod, Inc.
Decision Date2025-02-27
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

XOD Diathermia Radiofrequency Device is the device name listed in this FDA 510(k) record. The listed applicant is Xod, Inc.. It received FDA 510(k) clearance on 2025-02-27 under 510(k) number K242175. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XOD Diathermia Radiofrequency Device?

XOD Diathermia Radiofrequency Device is a medical device that received FDA 510(k) clearance on 2025-02-27. The listed applicant is Xod, Inc.. The 510(k) number is K242175.

When did XOD Diathermia Radiofrequency Device receive FDA 510(k) clearance?

XOD Diathermia Radiofrequency Device received FDA 510(k) clearance on 2025-02-27, under 510(k) number K242175.

Who is the listed applicant for XOD Diathermia Radiofrequency Device?

The FDA 510(k) record lists Xod, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for XOD Diathermia Radiofrequency Device?

The FDA product code for XOD Diathermia Radiofrequency Device is PBX.

Related Devices (Code: PBX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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