支架，頸動脈
PMA 核准號：P180010 · 2019-03-18
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器材摘要
Stent, carotid is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Gore & Associates, Inc.. It received FDA 510(k) clearance on 2019-03-18. The device is classified under product code NIM. It was reviewed by the CV advisory panel.
常見問題
What is the Stent, carotid?
Stent, carotid is a medical device that received FDA 510(k) clearance on 2019-03-18. The listed applicant is W. L. Gore & Associates, Inc..
When did Stent, carotid receive FDA 510(k) clearance?
The clearance date for Stent, carotid can be found in the official FDA records.
誰是Stent, 頸動脈的登記申請人？
The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
什麼是Stent, 頸動脈的FDA產品代碼？
FDA對於內瘻的產品代碼為NIM。
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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