Hornet 導絲，Hornet 10 導絲，Hornet 14 導絲
K 號：K152231 · 2016-02-12
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器材摘要
Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K152231. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire?
Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Boston Scientific Corporation. The 510(k) number is K152231.
When did Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire receive FDA 510(k) clearance?
Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire received FDA 510(k) clearance on 2016-02-12, under 510(k) number K152231.
Who is the listed applicant for Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire?
FDA 510(k) 記錄中將波士頓科學公司列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire?
The FDA product code for Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire is DQX.
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 Boston Scientific Corporation 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：DQX）
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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