恩塔里克 NI 飲食管系統
K 號：K241169 · 2024-11-22
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器材摘要
Entarik NI Feeding Tube System is the device name listed in this FDA 510(k) record. The listed applicant is Gravitas Medical, Inc.. It received FDA 510(k) clearance on 2024-11-22 under 510(k) number K241169. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Entarik NI Feeding Tube System?
Entarik NI Feeding Tube System is a medical device that received FDA 510(k) clearance on 2024-11-22. The listed applicant is Gravitas Medical, Inc.. The 510(k) number is K241169.
When did Entarik NI Feeding Tube System receive FDA 510(k) clearance?
Entarik NI Feeding Tube System received FDA 510(k) clearance on 2024-11-22, under 510(k) number K241169.
Who is the listed applicant for Entarik NI Feeding Tube System?
The FDA 510(k) record lists Gravitas Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Entarik NI Feeding Tube System?
The FDA product code for Entarik NI Feeding Tube System is KNT.
相關臨床試驗
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其他以 Gravitas Medical, Inc. 為申請人之記錄
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：KNT）
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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