DermiSphere 皮膚模板
K 號：K241904 · 2025-01-06
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器材摘要
DermiSphere Dermal Template is the device name listed in this FDA 510(k) record. The listed applicant is Fesariustherapeutics, Inc.. It received FDA 510(k) clearance on 2025-01-06 under 510(k) number K241904. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.
常見問題
What is the DermiSphere Dermal Template?
DermiSphere Dermal Template is a medical device that received FDA 510(k) clearance on 2025-01-06. The listed applicant is Fesariustherapeutics, Inc.. The 510(k) number is K241904.
When did DermiSphere Dermal Template receive FDA 510(k) clearance?
DermiSphere Dermal Template received FDA 510(k) clearance on 2025-01-06, under 510(k) number K241904.
Who is the listed applicant for DermiSphere Dermal Template?
The FDA 510(k) record lists Fesariustherapeutics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DermiSphere Dermal Template?
The FDA product code for DermiSphere Dermal Template is KGN.
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：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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