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FDA 510(k)

syngo Dynamics (Version VA41D)

K-Number: K242551 · 2025-04-03

ApplicantSiemens Healthcare GmbH
Decision Date2025-04-03
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

syngo Dynamics (Version VA41D) 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 2025-04-03 under 510(k) number K242551. 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 VA41D)?

syngo Dynamics (Version VA41D) is a medical device that received FDA 510(k) clearance on 2025-04-03. The listed applicant is Siemens Healthcare GmbH. The 510(k) number is K242551.

When did syngo Dynamics (Version VA41D) receive FDA 510(k) clearance?

syngo Dynamics (Version VA41D) received FDA 510(k) clearance on 2025-04-03, under 510(k) number K242551.

Who is the listed applicant for syngo Dynamics (Version VA41D)?

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 (Version VA41D)?

The FDA product code for syngo Dynamics (Version VA41D) is QIH.

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: QIH)

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.

K253794Prostate CoreLucida Medical, Ltd.K252571mdprostateMediaire GmbHK253902RealGUIDE3DIEMME SRLK253835AffinityHermes Medical Solutions ABK260980cmAngio® V2.0Curemetrix, Inc.K261210Cleerly PlaqueCleerly, Inc.

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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