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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 a medical device manufactured by MeVis Medical Solutions AG. It received FDA 510(k) clearance on 2021-02-23 under approval 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. It is manufactured by MeVis Medical Solutions AG. The 510(k) number is K201501.

When was Veolity approved by the FDA?

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

What company makes Veolity?

Veolity is manufactured by MeVis Medical Solutions AG.

What is the FDA product code for Veolity?

The FDA product code for Veolity is OEB.

Other Devices by MeVis Medical Solutions AG

K232045MeVis Liver Suite

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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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