syngo Dynamics (Version VA40E)
K-Number: K220832 · 2022-05-20
ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2022-05-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
syngo Dynamics (Version VA40E) is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2022-05-20 under approval number K220832. 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 VA40E)?
syngo Dynamics (Version VA40E) is a medical device that received FDA 510(k) clearance on 2022-05-20. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K220832.
When was syngo Dynamics (Version VA40E) approved by the FDA?
syngo Dynamics (Version VA40E) received FDA 510(k) clearance on 2022-05-20, under approval number K220832.
What company makes syngo Dynamics (Version VA40E)?
syngo Dynamics (Version VA40E) is manufactured by Siemens Medical Solutions USA, Inc..
What is the FDA product code for syngo Dynamics (Version VA40E)?
The FDA product code for syngo Dynamics (Version VA40E) is LLZ.
Other Devices by Siemens Medical Solutions USA, Inc.
Related Devices (Code: LLZ)
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.