心臟消融經皮針狀電極
PMA 核准號：P040036 · 2026-09-15
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器材摘要
Cardiac ablation percutaneous catheter is the device name listed in this FDA 510(k) record. The listed applicant is Biosense Webster, Inc.. It received FDA 510(k) clearance on 2026-09-15. The device is classified under product code LPB. It was reviewed by the CV advisory panel.
常見問題
What is the Cardiac ablation percutaneous catheter?
Cardiac ablation percutaneous catheter is a medical device that received FDA 510(k) clearance on 2026-09-15. The listed applicant is Biosense Webster, Inc..
When did Cardiac ablation percutaneous catheter receive FDA 510(k) clearance?
The clearance date for Cardiac ablation percutaneous catheter can be found in the official FDA records.
誰是Cardiac ablation percutaneous catheter的登記申請人？
The FDA 510(k) record lists Biosense Webster, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為Cardiac ablation percutaneous catheter是什麼？
FDA產品代碼為Cardiac ablation percutaneous catheter的是LPB。
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。
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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