薩維安DLVR導絲，薩維安FLX導絲
K 號：K180726 · 2018-06-18
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器材摘要
Savion DLVR Guidewire, Savion FLX Guidewire is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific, Inc.. It received FDA 510(k) clearance on 2018-06-18 under 510(k) number K180726. 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 Savion DLVR Guidewire, Savion FLX Guidewire?
Savion DLVR Guidewire, Savion FLX Guidewire is a medical device that received FDA 510(k) clearance on 2018-06-18. The listed applicant is Boston Scientific, Inc.. The 510(k) number is K180726.
When did Savion DLVR Guidewire, Savion FLX Guidewire receive FDA 510(k) clearance?
Savion DLVR Guidewire, Savion FLX Guidewire received FDA 510(k) clearance on 2018-06-18, under 510(k) number K180726.
Who is the listed applicant for Savion DLVR Guidewire, Savion FLX Guidewire?
The FDA 510(k) record lists Boston Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Savion DLVR Guidewire, Savion FLX Guidewire?
The FDA product code for Savion DLVR Guidewire, Savion FLX Guidewire is DQX.
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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
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