BD Vacutainer® 一次性持桿器
K 號：K242320 · 2024-11-01
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器材摘要
BD Vacutainer® One Use Holder 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 2024-11-01 under 510(k) number K242320. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BD Vacutainer® One Use Holder?
BD Vacutainer® One Use Holder is a medical device that received FDA 510(k) clearance on 2024-11-01. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K242320.
When did BD Vacutainer® One Use Holder receive FDA 510(k) clearance?
BD Vacutainer® One Use Holder received FDA 510(k) clearance on 2024-11-01, under 510(k) number K242320.
Who is the listed applicant for BD Vacutainer® One Use Holder?
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 Vacutainer® One Use Holder?
The FDA product code for BD Vacutainer® One Use Holder is JKA.
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 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：JKA）
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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