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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 the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2023-03-21 under 510(k) 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. The listed applicant is Siemens Healthcare GmbH. The 510(k) number is K230561.

When did Syngo Carbon Space VA30A receive FDA 510(k) clearance?

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

Who is the listed applicant for Syngo Carbon Space VA30A?

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

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

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

Other records listing Siemens Healthcare GmbH 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.

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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

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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