BD MAX Check-Points CPO
K 號：K190613 · 2019-08-29
廣告
器材摘要
BD MAX Check-Points CPO is the device name listed in this FDA 510(k) record. The listed applicant is Check-Points Health B.V.. It received FDA 510(k) clearance on 2019-08-29 under 510(k) number K190613. The device is classified under product code POC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the BD MAX Check-Points CPO?
BD MAX Check-Points CPO is a medical device that received FDA 510(k) clearance on 2019-08-29. The listed applicant is Check-Points Health B.V.. The 510(k) number is K190613.
When did BD MAX Check-Points CPO receive FDA 510(k) clearance?
BD MAX Check-Points CPO received FDA 510(k) clearance on 2019-08-29, under 510(k) number K190613.
Who is the listed applicant for BD MAX Check-Points CPO?
The FDA 510(k) record lists Check-Points Health B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD MAX Check-Points CPO?
The FDA product code for BD MAX Check-Points CPO is POC.
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。
相關器械（代碼：POC）
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。
廣告