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FDA 510(k)

Clarus Viewer

K-Number: K222757 · 2023-02-24

ApplicantClarus Viewer Corporation
Decision Date2023-02-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Clarus Viewer is a medical device manufactured by Clarus Viewer Corporation. It received FDA 510(k) clearance on 2023-02-24 under approval 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. It is manufactured by Clarus Viewer Corporation. The 510(k) number is K222757.

When was Clarus Viewer approved by the FDA?

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

What company makes Clarus Viewer?

Clarus Viewer is manufactured by Clarus Viewer Corporation.

What is the FDA product code for Clarus Viewer?

The FDA product code for Clarus Viewer is LLZ.

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Official Source

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