FDA 510(k)

InnovaMatrix®FD

K番号: K241866 · 2024-07-26

決定日2024-07-26

製品コードKGN

決定大幅同等

医療機器の概要

InnovaMatrix®FD is the device name listed in this FDA 510(k) record. The listed applicant is Convatec Triad Life Sciences, LLC. It received FDA 510(k) clearance on 2024-07-26 under 510(k) number K241866. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

よくある質問

What is the InnovaMatrix®FD?

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

When did InnovaMatrix®FD receive FDA 510(k) clearance?

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

Who is the listed applicant for InnovaMatrix®FD?

The FDA 510(k) record lists Convatec Triad Life Sciences, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for InnovaMatrix®FD?

The FDA product code for InnovaMatrix®FD is KGN.

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InnovaMatrix®FD

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：KGN）

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