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FDA 510(k)

MR5 Activ Pro

K-Number: K254024 · 2026-05-19

ApplicantMulti Radiance Medical, Inc.
Decision Date2026-05-19
Product CodeNHN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MR5 Activ Pro is the device name listed in this FDA 510(k) record. The listed applicant is Multi Radiance Medical, Inc.. It received FDA 510(k) clearance on 2026-05-19 under 510(k) number K254024. The device is classified under product code NHN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MR5 Activ Pro?

MR5 Activ Pro is a medical device that received FDA 510(k) clearance on 2026-05-19. The listed applicant is Multi Radiance Medical, Inc.. The 510(k) number is K254024.

When did MR5 Activ Pro receive FDA 510(k) clearance?

MR5 Activ Pro received FDA 510(k) clearance on 2026-05-19, under 510(k) number K254024.

Who is the listed applicant for MR5 Activ Pro?

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

What is the FDA product code for MR5 Activ Pro?

The FDA product code for MR5 Activ Pro is NHN.

Other records listing Multi Radiance Medical, Inc. as applicant

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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Related Devices (Code: NHN)

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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