FDA 510(k)

syngo Dynamics Version VA30

K-Number: K171053 · 2017-06-01

Decision Date2017-06-01

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo Dynamics Version VA30 is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2017-06-01 under approval number K171053. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the syngo Dynamics Version VA30?

syngo Dynamics Version VA30 is a medical device that received FDA 510(k) clearance on 2017-06-01. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K171053.

When was syngo Dynamics Version VA30 approved by the FDA?

syngo Dynamics Version VA30 received FDA 510(k) clearance on 2017-06-01, under approval number K171053.

What company makes syngo Dynamics Version VA30?

syngo Dynamics Version VA30 is manufactured by Siemens Healthcare GmbH.

What is the FDA product code for syngo Dynamics Version VA30?

The FDA product code for syngo Dynamics Version VA30 is LLZ.

Other Devices by Siemens Healthcare GmbH

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.