FDA 510(k)

syngo.CT Clinical Extensions

K-Number: K173625 · 2018-03-08

ApplicantSiemens Medical Solutions USA, Inc.

Decision Date2018-03-08

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo.CT Clinical Extensions is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2018-03-08 under approval number K173625. 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 Clinical Extensions?

syngo.CT Clinical Extensions is a medical device that received FDA 510(k) clearance on 2018-03-08. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K173625.

When was syngo.CT Clinical Extensions approved by the FDA?

syngo.CT Clinical Extensions received FDA 510(k) clearance on 2018-03-08, under approval number K173625.

What company makes syngo.CT Clinical Extensions?

syngo.CT Clinical Extensions is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for syngo.CT Clinical Extensions?

The FDA product code for syngo.CT Clinical Extensions is JAK.

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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.