賈森膠膜
K 號：K242817 · 2025-12-12
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器材摘要
Jason membrane is the device name listed in this FDA 510(k) record. The listed applicant is Botiss Biomaterials GmbH. It received FDA 510(k) clearance on 2025-12-12 under 510(k) number K242817. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Jason membrane?
Jason membrane is a medical device that received FDA 510(k) clearance on 2025-12-12. The listed applicant is Botiss Biomaterials GmbH. The 510(k) number is K242817.
When did Jason membrane receive FDA 510(k) clearance?
Jason membrane received FDA 510(k) clearance on 2025-12-12, under 510(k) number K242817.
Who is the listed applicant for Jason membrane?
The FDA 510(k) record lists Botiss Biomaterials GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Jason membrane?
The FDA product code for Jason membrane is NPL.
相關臨床試驗
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。
相關器械（代碼：NPL）
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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