FDA 510(k)

syngo®.via protoNeo (Version VA20)

K-Number: K173378 · 2017-11-20

Decision Date2017-11-20

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo®.via protoNeo (Version VA20) is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2017-11-20 under approval number K173378. 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®.via protoNeo (Version VA20)?

syngo®.via protoNeo (Version VA20) is a medical device that received FDA 510(k) clearance on 2017-11-20. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K173378.

When was syngo®.via protoNeo (Version VA20) approved by the FDA?

syngo®.via protoNeo (Version VA20) received FDA 510(k) clearance on 2017-11-20, under approval number K173378.

What company makes syngo®.via protoNeo (Version VA20)?

syngo®.via protoNeo (Version VA20) is manufactured by Siemens Healthcare GmbH.

What is the FDA product code for syngo®.via protoNeo (Version VA20)?

The FDA product code for syngo®.via protoNeo (Version VA20) is LLZ.

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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.