FDA 510(k)

syngo.via View&GO

K-Number: K221501 · 2022-10-14

Decision Date2022-10-14

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo.via View&GO is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2022-10-14 under approval number K221501. 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?

syngo.via View&GO is a medical device that received FDA 510(k) clearance on 2022-10-14. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K221501.

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

syngo.via View&GO received FDA 510(k) clearance on 2022-10-14, under approval number K221501.

What company makes syngo.via View&GO?

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

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

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

Other Devices by Siemens Healthcare GmbH

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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.