BD BACTEC FXI 培養系統
K 號：K260213 · 2026-05-28
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器材摘要
BD BACTEC FXI Culture System is the device name listed in this FDA 510(k) record. The listed applicant is BD Diagnostic Systems. It received FDA 510(k) clearance on 2026-05-28 under 510(k) number K260213. The device is classified under product code MDB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BD BACTEC FXI Culture System?
BD BACTEC FXI Culture System is a medical device that received FDA 510(k) clearance on 2026-05-28. The listed applicant is BD Diagnostic Systems. The 510(k) number is K260213.
When did BD BACTEC FXI Culture System receive FDA 510(k) clearance?
BD BACTEC FXI Culture System received FDA 510(k) clearance on 2026-05-28, under 510(k) number K260213.
Who is the listed applicant for BD BACTEC FXI Culture System?
The FDA 510(k) record lists BD Diagnostic Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD BACTEC FXI Culture System?
The FDA product code for BD BACTEC FXI Culture System is MDB.
相關臨床試驗
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相關器械（代碼：MDB）
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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