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FDA 510(k)

Limbus Contour

K-Number: K241837 · 2024-10-09

ApplicantLimbus Ai, Inc.
Decision Date2024-10-09
Product CodeQKB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Limbus Contour is a medical device manufactured by Limbus Ai, Inc.. It received FDA 510(k) clearance on 2024-10-09 under approval number K241837. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Limbus Contour?

Limbus Contour is a medical device that received FDA 510(k) clearance on 2024-10-09. It is manufactured by Limbus Ai, Inc.. The 510(k) number is K241837.

When was Limbus Contour approved by the FDA?

Limbus Contour received FDA 510(k) clearance on 2024-10-09, under approval number K241837.

What company makes Limbus Contour?

Limbus Contour is manufactured by Limbus Ai, Inc..

What is the FDA product code for Limbus Contour?

The FDA product code for Limbus Contour is QKB.

Other Devices by Limbus Ai, Inc.

K201232Limbus Contour K230575Limbus Contour

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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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