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FDA 510(k)

syngo.via RT Image Suite

K-Number: K162370 · 2016-10-25

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date2016-10-25
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

syngo.via RT Image Suite is a medical device manufactured by Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-10-25 under approval number K162370. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the syngo.via RT Image Suite?

syngo.via RT Image Suite is a medical device that received FDA 510(k) clearance on 2016-10-25. It is manufactured by Siemens Medical Solutions USA, Inc.. The 510(k) number is K162370.

When was syngo.via RT Image Suite approved by the FDA?

syngo.via RT Image Suite received FDA 510(k) clearance on 2016-10-25, under approval number K162370.

What company makes syngo.via RT Image Suite?

syngo.via RT Image Suite is manufactured by Siemens Medical Solutions USA, Inc..

What is the FDA product code for syngo.via RT Image Suite?

The FDA product code for syngo.via RT Image Suite is MUJ.

Related Clinical Trials

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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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