心臟藥物釋放支架
PMA 核准號：P100023 · 2016-02-16
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器材摘要
Coronary drug-eluting stent is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2016-02-16. The device is classified under product code NIQ. It was reviewed by the CV advisory panel.
常見問題
What is the Coronary drug-eluting stent?
Coronary drug-eluting stent is a medical device that received FDA 510(k) clearance on 2016-02-16. The listed applicant is Boston Scientific Corp.
When did Coronary drug-eluting stent receive FDA 510(k) clearance?
The clearance date for Coronary drug-eluting stent can be found in the official FDA records.
誰是Coronary藥物滲透支架的登記申請人？
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？Coronary drug-eluting stent？
FDA對冠狀藥物涂裝支架的產品代碼為NIQ。
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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