Emprint SX 消融平台及配件
K 號:K171358 · 2017-09-01
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器材摘要
常見問題
What is the Emprint SX Ablation Platform and Accessories?
Emprint SX Ablation Platform and Accessories is a medical device that received FDA 510(k) clearance on 2017-09-01. The listed applicant is Coviden, LLC. The 510(k) number is K171358.
When did Emprint SX Ablation Platform and Accessories receive FDA 510(k) clearance?
Emprint SX Ablation Platform and Accessories received FDA 510(k) clearance on 2017-09-01, under 510(k) number K171358.
Who is the listed applicant for Emprint SX Ablation Platform and Accessories?
The FDA 510(k) record lists Coviden, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Emprint SX Ablation Platform and Accessories?
The FDA product code for Emprint SX Ablation Platform and Accessories is NEY.
相關臨床試驗
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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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