FDA 510(k)

syngo Dynamics (VA41F)

Número K: K253689 · 2026-04-10

Data da decisão2026-04-10

Código do produtoQIH

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

syngo Dynamics (VA41F) 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 2026-04-10 under 510(k) number K253689. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the syngo Dynamics (VA41F)?

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

When did syngo Dynamics (VA41F) receive FDA 510(k) clearance?

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

Who is the listed applicant for syngo Dynamics (VA41F)?

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 Dynamics (VA41F)?

The FDA product code for syngo Dynamics (VA41F) is QIH.

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Fonte oficial

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