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FDA 510(k)

VSI HoloMedicine

K-Number: K213215 · 2022-11-25

ApplicantApoqlar GmbH
Decision Date2022-11-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VSI HoloMedicine is a medical device manufactured by Apoqlar GmbH. It received FDA 510(k) clearance on 2022-11-25 under approval number K213215. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VSI HoloMedicine?

VSI HoloMedicine is a medical device that received FDA 510(k) clearance on 2022-11-25. It is manufactured by Apoqlar GmbH. The 510(k) number is K213215.

When was VSI HoloMedicine approved by the FDA?

VSI HoloMedicine received FDA 510(k) clearance on 2022-11-25, under approval number K213215.

What company makes VSI HoloMedicine?

VSI HoloMedicine is manufactured by Apoqlar GmbH.

What is the FDA product code for VSI HoloMedicine?

The FDA product code for VSI HoloMedicine is LLZ.

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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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