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FDA 510(k)

InnovaMatrix®FD

K-Number: K241866 · 2024-07-26

ApplicantConvatec Triad Life Sciences, LLC
Decision Date2024-07-26
Product CodeKGN
DecisionSubstantially Equivalent

Device Summary

InnovaMatrix®FD is a medical device manufactured by Convatec Triad Life Sciences, LLC. It received FDA 510(k) clearance on 2024-07-26 under approval number K241866. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InnovaMatrix®FD?

InnovaMatrix®FD is a medical device that received FDA 510(k) clearance on 2024-07-26. It is manufactured by Convatec Triad Life Sciences, LLC. The 510(k) number is K241866.

When was InnovaMatrix®FD approved by the FDA?

InnovaMatrix®FD received FDA 510(k) clearance on 2024-07-26, under approval number K241866.

What company makes InnovaMatrix®FD?

InnovaMatrix®FD is manufactured by Convatec Triad Life Sciences, LLC.

What is the FDA product code for InnovaMatrix®FD?

The FDA product code for InnovaMatrix®FD is KGN.

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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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