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FDA 510(k)

syngo.via View&GO VA40A

K-Number: K230196 · 2023-02-13

ApplicantSiemens Healthcare GmbH
Decision Date2023-02-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

syngo.via View&GO VA40A is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare GmbH. It received FDA 510(k) clearance on 2023-02-13 under 510(k) 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. The listed applicant is Siemens Healthcare GmbH. The 510(k) number is K230196.

When did syngo.via View&GO VA40A receive FDA 510(k) clearance?

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

Who is the listed applicant for syngo.via View&GO VA40A?

The FDA 510(k) record lists Siemens Healthcare GmbH as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Siemens Healthcare GmbH as applicant

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Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLCK261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific CorporationK262143ImageGrid StreamVueCandelis, Inc.

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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