BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube
K 號:K160657 · 2016-09-23
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器材摘要
常見問題
What is the BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube?
BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube is a medical device that received FDA 510(k) clearance on 2016-09-23. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K160657.
When did BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube receive FDA 510(k) clearance?
BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube received FDA 510(k) clearance on 2016-09-23, under 510(k) number K160657.
Who is the listed applicant for BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube?
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 Barricor Lithium Heparin Plasma Blood Collection Tube?
The FDA product code for BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube is JKA.
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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: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。
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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