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FDA 510(k)

Syngo Dynamics (Version VA40F)

K-Number: K222428 · 2022-11-14

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-11-14
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Syngo Dynamics (Version VA40F) is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-11-14 under approval number K222428. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Syngo Dynamics (Version VA40F)?

Syngo Dynamics (Version VA40F) is a medical device that received FDA 510(k) clearance on 2022-11-14. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K222428.

When was Syngo Dynamics (Version VA40F) approved by the FDA?

Syngo Dynamics (Version VA40F) received FDA 510(k) clearance on 2022-11-14, under approval number K222428.

What company makes Syngo Dynamics (Version VA40F)?

Syngo Dynamics (Version VA40F) is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for Syngo Dynamics (Version VA40F)?

The FDA product code for Syngo Dynamics (Version VA40F) is QIH.

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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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