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FDA 510(k)

syngo.CT Neuro Perfusion

K-Number: K202213 · 2020-10-11

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2020-10-11
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

syngo.CT Neuro Perfusion is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2020-10-11 under approval number K202213. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the syngo.CT Neuro Perfusion?

syngo.CT Neuro Perfusion is a medical device that received FDA 510(k) clearance on 2020-10-11. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K202213.

When was syngo.CT Neuro Perfusion approved by the FDA?

syngo.CT Neuro Perfusion received FDA 510(k) clearance on 2020-10-11, under approval number K202213.

What company makes syngo.CT Neuro Perfusion?

syngo.CT Neuro Perfusion is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for syngo.CT Neuro Perfusion?

The FDA product code for syngo.CT Neuro Perfusion is JAK.

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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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