FDA 510(k)

syngo.plaza

K-Number: K180563 · 2018-04-25

Decision Date2018-04-25

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

syngo.plaza is a medical device manufactured by Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2018-04-25 under approval number K180563. 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.plaza?

syngo.plaza is a medical device that received FDA 510(k) clearance on 2018-04-25. It is manufactured by Siemens Healthcare GmbH. The 510(k) number is K180563.

When was syngo.plaza approved by the FDA?

syngo.plaza received FDA 510(k) clearance on 2018-04-25, under approval number K180563.

What company makes syngo.plaza?

syngo.plaza is manufactured by Siemens Healthcare GmbH.

What is the FDA product code for syngo.plaza?

The FDA product code for syngo.plaza 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.