FDA 510(k)

syngo Dynamics (Version VA41D)

K-Number: K242551 · 2025-04-03

Decision Date2025-04-03

Product CodeQIH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo Dynamics (Version VA41D) is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2025-04-03 under approval 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. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K242551.

When was syngo Dynamics (Version VA41D) approved by the FDA?

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

What company makes syngo Dynamics (Version VA41D)?

syngo Dynamics (Version VA41D) is manufactured by Siemens Healthcare GmbH.

What is the FDA product code for syngo Dynamics (Version VA41D)?

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

Other Devices by Siemens Healthcare GmbH

K161685syngo®.via protoNeo (Version VA10A) K173378syngo®.via protoNeo (Version VA20) K171053syngo Dynamics Version VA30 K170221syngo.CT Cardiac Planning K182208syngo.via View&GO (Version VA10A) K180563syngo.plaza

View all 30 devices →

Related Devices (Code: QIH)

K191647QLAB Advanced Quantification SoftwarePhilips Health Care K191171EchoGo CoreUltromics, Ltd. K201195syngo.via MI Workflows, syngo MBFSiemens Medical Solutions USA, Inc. K202013WRDensity by Whiterabbit.aiWhiterabbit.Ai, Inc. K202546LVivo SeamlessDia Imaging Analysis, Ltd. K193283AI-Rad Companion Prostate MRSiemens Medical Solutions USA, 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.