FDA 510(k)

Clarus Viewer

K-Number: K222757 · 2023-02-24

Decision Date2023-02-24

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Clarus Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Clarus Viewer Corporation. It received FDA 510(k) clearance on 2023-02-24 under 510(k) number K222757. 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 Clarus Viewer?

Clarus Viewer is a medical device that received FDA 510(k) clearance on 2023-02-24. The listed applicant is Clarus Viewer Corporation. The 510(k) number is K222757.

When did Clarus Viewer receive FDA 510(k) clearance?

Clarus Viewer received FDA 510(k) clearance on 2023-02-24, under 510(k) number K222757.

Who is the listed applicant for Clarus Viewer?

The FDA 510(k) record lists Clarus Viewer Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Clarus Viewer?

The FDA product code for Clarus Viewer is LLZ.

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, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

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.