FDA 510(k)

syngo Dynamics (VA41F)

K-Number: K253689 · 2026-04-10

Decision Date2026-04-10

Product CodeQIH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo Dynamics (VA41F) is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2026-04-10 under approval number K253689. 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 (VA41F)?

syngo Dynamics (VA41F) is a medical device that received FDA 510(k) clearance on 2026-04-10. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K253689.

When was syngo Dynamics (VA41F) approved by the FDA?

syngo Dynamics (VA41F) received FDA 510(k) clearance on 2026-04-10, under approval number K253689.

What company makes syngo Dynamics (VA41F)?

syngo Dynamics (VA41F) is manufactured by Siemens Healthcare GmbH.

What is the FDA product code for syngo Dynamics (VA41F)?

The FDA product code for syngo Dynamics (VA41F) 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.