IntelliCuff
K 號：K150893 · 2016-01-29
廣告
器材摘要
IntelliCuff is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Medical AG. It received FDA 510(k) clearance on 2016-01-29 under 510(k) number K150893. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the IntelliCuff?
IntelliCuff is a medical device that received FDA 510(k) clearance on 2016-01-29. The listed applicant is Hamilton Medical AG. The 510(k) number is K150893.
When did IntelliCuff receive FDA 510(k) clearance?
IntelliCuff received FDA 510(k) clearance on 2016-01-29, under 510(k) number K150893.
Who is the listed applicant for IntelliCuff?
The FDA 510(k) record lists Hamilton Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IntelliCuff?
The FDA product code for IntelliCuff is BSK.
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 Hamilton Medical AG 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：BSK）
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