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FDA 510(k)

aiCockpit AI Viewer

K-Number: K241546 · 2025-02-26

ApplicantFovia, Inc.
Decision Date2025-02-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

aiCockpit AI Viewer is a medical device manufactured by Fovia, Inc.. It received FDA 510(k) clearance on 2025-02-26 under approval number K241546. 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 aiCockpit AI Viewer?

aiCockpit AI Viewer is a medical device that received FDA 510(k) clearance on 2025-02-26. It is manufactured by Fovia, Inc.. The 510(k) number is K241546.

When was aiCockpit AI Viewer approved by the FDA?

aiCockpit AI Viewer received FDA 510(k) clearance on 2025-02-26, under approval number K241546.

What company makes aiCockpit AI Viewer?

aiCockpit AI Viewer is manufactured by Fovia, Inc..

What is the FDA product code for aiCockpit AI Viewer?

The FDA product code for aiCockpit AI Viewer is LLZ.

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Official Source

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