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FDA 510(k)

Veolity

K-Number: K201501 · 2021-02-23

ApplicantMeVis Medical Solutions AG
Decision Date2021-02-23
Product CodeOEB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Veolity is the device name listed in this FDA 510(k) record. The listed applicant is MeVis Medical Solutions AG. It received FDA 510(k) clearance on 2021-02-23 under 510(k) number K201501. The device is classified under product code OEB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Veolity?

Veolity is a medical device that received FDA 510(k) clearance on 2021-02-23. The listed applicant is MeVis Medical Solutions AG. The 510(k) number is K201501.

When did Veolity receive FDA 510(k) clearance?

Veolity received FDA 510(k) clearance on 2021-02-23, under 510(k) number K201501.

Who is the listed applicant for Veolity?

The FDA 510(k) record lists MeVis Medical Solutions AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Veolity?

The FDA product code for Veolity is OEB.

Other records listing MeVis Medical Solutions AG 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.

K260576MeVis AVM ContourK232045MeVis Liver Suite

Related Devices (Code: OEB)

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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