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FDA 510(k)

Syngo Carbon Space VA30A

K-Number: K230561 · 2023-03-21

ApplicantSiemens Healthcare GmbH
Decision Date2023-03-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Syngo Carbon Space VA30A is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2023-03-21 under approval number K230561. 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 Syngo Carbon Space VA30A?

Syngo Carbon Space VA30A is a medical device that received FDA 510(k) clearance on 2023-03-21. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K230561.

When was Syngo Carbon Space VA30A approved by the FDA?

Syngo Carbon Space VA30A received FDA 510(k) clearance on 2023-03-21, under approval number K230561.

What company makes Syngo Carbon Space VA30A?

Syngo Carbon Space VA30A is manufactured by Siemens Healthcare GmbH.

What is the FDA product code for Syngo Carbon Space VA30A?

The FDA product code for Syngo Carbon Space VA30A is LLZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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