FDA 510(k)

VSI HoloMedicine

K-Number: K213215 · 2022-11-25

Decision Date2022-11-25

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

VSI HoloMedicine is the device name listed in this FDA 510(k) record. The listed applicant is Apoqlar GmbH. It received FDA 510(k) clearance on 2022-11-25 under 510(k) 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. The listed applicant is Apoqlar GmbH. The 510(k) number is K213215.

When did VSI HoloMedicine receive FDA 510(k) clearance?

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

Who is the listed applicant for VSI HoloMedicine?

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

What is the FDA product code for VSI HoloMedicine?

The FDA product code for VSI HoloMedicine is LLZ.

Related Devices (Code: LLZ)

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.