FLEX 麻醉微波消融系統及附件
K 號:K163118 · 2017-03-09
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器材摘要
常見問題
What is the FLEX Microwave Ablation System and Accessories?
FLEX Microwave Ablation System and Accessories is a medical device that received FDA 510(k) clearance on 2017-03-09. The listed applicant is Neuwave Medical, Inc.. The 510(k) number is K163118.
When did FLEX Microwave Ablation System and Accessories receive FDA 510(k) clearance?
FLEX Microwave Ablation System and Accessories received FDA 510(k) clearance on 2017-03-09, under 510(k) number K163118.
Who is the listed applicant for FLEX Microwave Ablation System and Accessories?
The FDA 510(k) record lists Neuwave Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEX Microwave Ablation System and Accessories?
The FDA product code for FLEX Microwave Ablation System and Accessories is NEY.
相關臨床試驗
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其他以 Neuwave Medical, Inc. 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:NEY)
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。
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