InnovaMatrix®FD
K 號：K241866 · 2024-07-26
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器材摘要
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.
常見問題
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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相關器械（代碼：KGN）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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