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FDA 510(k)

Mural Clinical Viewer

K-Number: K222586 · 2022-12-21

ApplicantGe Medical Systems Information Technologies, Inc.
Decision Date2022-12-21
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Mural Clinical Viewer is a medical device manufactured by Ge Medical Systems Information Technologies, Inc.. It received FDA 510(k) clearance on 2022-12-21 under approval number K222586. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Mural Clinical Viewer?

Mural Clinical Viewer is a medical device that received FDA 510(k) clearance on 2022-12-21. It is manufactured by Ge Medical Systems Information Technologies, Inc.. The 510(k) number is K222586.

When was Mural Clinical Viewer approved by the FDA?

Mural Clinical Viewer received FDA 510(k) clearance on 2022-12-21, under approval number K222586.

What company makes Mural Clinical Viewer?

Mural Clinical Viewer is manufactured by Ge Medical Systems Information Technologies, Inc..

What is the FDA product code for Mural Clinical Viewer?

The FDA product code for Mural Clinical Viewer is MHX.

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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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