BD Plastipak™針筒
K 號：K251350 · 2025-07-29
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決定日期2025-07-29
產品代碼FMF
諮詢委員會醫療設備規範文本翻譯如下：
HO
注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於
器材摘要
BD Plastipak™ Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2025-07-29 under 510(k) number K251350. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BD Plastipak™ Syringe?
BD Plastipak™ Syringe is a medical device that received FDA 510(k) clearance on 2025-07-29. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K251350.
When did BD Plastipak™ Syringe receive FDA 510(k) clearance?
BD Plastipak™ Syringe received FDA 510(k) clearance on 2025-07-29, under 510(k) number K251350.
Who is the listed applicant for BD Plastipak™ Syringe?
The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD Plastipak™ Syringe?
The FDA product code for BD Plastipak™ Syringe is FMF.
相關臨床試驗
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其他以 Becton, Dickinson and Company 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：FMF）
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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