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FDA 510(k)

BD MAX 肠道細菌檢測組合, BD MAX 扩展性肠道細菌檢測組合

K 號:K214122 · 2022-07-28

決定日期2022-07-28
產品代碼PCI
諮詢委員會MI (請提供完整的描述文本,以便進行翻譯。)
決定相當於

器材摘要

BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel 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 2022-07-28 under 510(k) number K214122. The device is classified under product code PCI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel?

BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel is a medical device that received FDA 510(k) clearance on 2022-07-28. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K214122.

When did BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel receive FDA 510(k) clearance?

BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel received FDA 510(k) clearance on 2022-07-28, under 510(k) number K214122.

Who is the listed applicant for BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel?

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 MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel?

The FDA product code for BD MAX Enteric Bacterial Panel, BD MAX Extended Enteric Bacterial Panel is PCI.

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其他以 Becton, Dickinson and Company 為申請人之記錄

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相關器械(代碼:PCI)

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

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