Nutricair 內腸注射器配ENFit
K 號：K231300 · 2023-10-06
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器材摘要
Nutricair Enteral Syringe with ENFit is the device name listed in this FDA 510(k) record. The listed applicant is Cair Lgl. It received FDA 510(k) clearance on 2023-10-06 under 510(k) number K231300. The device is classified under product code PNR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Nutricair Enteral Syringe with ENFit?
Nutricair Enteral Syringe with ENFit is a medical device that received FDA 510(k) clearance on 2023-10-06. The listed applicant is Cair Lgl. The 510(k) number is K231300.
When did Nutricair Enteral Syringe with ENFit receive FDA 510(k) clearance?
Nutricair Enteral Syringe with ENFit received FDA 510(k) clearance on 2023-10-06, under 510(k) number K231300.
Who is the listed applicant for Nutricair Enteral Syringe with ENFit?
The FDA 510(k) record lists Cair Lgl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nutricair Enteral Syringe with ENFit?
The FDA product code for Nutricair Enteral Syringe with ENFit is PNR.
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。
其他以 Cair Lgl 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：PNR）
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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