藥物釋放永久性右心室（RV）或右心房（RA）起搏器電極
PMA 核准號：P950001 · 2021-04-02
廣告
器材摘要
Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific. It received FDA 510(k) clearance on 2021-04-02. The device is classified under product code NVN. It was reviewed by the CV advisory panel.
常見問題
What is the Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes?
Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes is a medical device that received FDA 510(k) clearance on 2021-04-02. The listed applicant is Boston Scientific.
When did Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes receive FDA 510(k) clearance?
The clearance date for Drug eluting permanent right ventricular (RV) or right atrial (RA) pacemaker electrodes can be found in the official FDA records.
誰是藥物釋放永久性右心室（RV）或右心房（RA）起搏器電極的登記申請人？
FDA 510(k) 記錄將波士頓科學公司列為申請人。這並不單獨確立設備製造商。
FDA產品代碼是什麼？用於藥物釋放永久性右心室（RV）或右心房（RA）起搏器電極？
FDA 藥物滲透永久性右心室（RV）或右心房（RA）起搏器電極的產品代碼為 NVN。
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。
廣告