極光RF消融系統
K 號：K181864 · 2019-01-02
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器材摘要
Polaris RF Ablation System is the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Company, Inc.. It received FDA 510(k) clearance on 2019-01-02 under 510(k) number K181864. The device is classified under product code GXD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Polaris RF Ablation System?
Polaris RF Ablation System is a medical device that received FDA 510(k) clearance on 2019-01-02. The listed applicant is Baylis Medical Company, Inc.. The 510(k) number is K181864.
When did Polaris RF Ablation System receive FDA 510(k) clearance?
Polaris RF Ablation System received FDA 510(k) clearance on 2019-01-02, under 510(k) number K181864.
Who is the listed applicant for Polaris RF Ablation System?
The FDA 510(k) record lists Baylis Medical Company, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Polaris RF Ablation System?
The FDA product code for Polaris RF Ablation System is GXD.
相關臨床試驗
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其他以 Baylis Medical Company, 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：GXD）
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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