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FDA 510(k)

Syngo Dynamics (Version VA40F)

K-Number: K222428 · 2022-11-14

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-11-14
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Syngo Dynamics (Version VA40F) is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-11-14 under 510(k) number K222428. 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 VA40F)?

Syngo Dynamics (Version VA40F) is a medical device that received FDA 510(k) clearance on 2022-11-14. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K222428.

When did Syngo Dynamics (Version VA40F) receive FDA 510(k) clearance?

Syngo Dynamics (Version VA40F) received FDA 510(k) clearance on 2022-11-14, under 510(k) number K222428.

Who is the listed applicant for Syngo Dynamics (Version VA40F)?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Syngo Dynamics (Version VA40F)?

The FDA product code for Syngo Dynamics (Version VA40F) 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.

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