FDA 510(k)

syngo.via View&GO VA40A

K-Number: K230196 · 2023-02-13

Decision Date2023-02-13

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo.via View&GO VA40A is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2023-02-13 under approval number K230196. 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 View&GO VA40A?

syngo.via View&GO VA40A is a medical device that received FDA 510(k) clearance on 2023-02-13. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K230196.

When was syngo.via View&GO VA40A approved by the FDA?

syngo.via View&GO VA40A received FDA 510(k) clearance on 2023-02-13, under approval number K230196.

What company makes syngo.via View&GO VA40A?

syngo.via View&GO VA40A is manufactured by Siemens Healthcare GmbH.

What is the FDA product code for syngo.via View&GO VA40A?

The FDA product code for syngo.via View&GO VA40A is LLZ.

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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.