支架，股浅動脈，藥物釋放
PMA 核准號：P100022 · 2026-03-25
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器材摘要
Stent, superficial femoral artery, drug-eluting is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ireland, Ltd.. It received FDA 510(k) clearance on 2026-03-25. The device is classified under product code NIU. It was reviewed by the CV advisory panel.
常見問題
What is the Stent, superficial femoral artery, drug-eluting?
Stent, superficial femoral artery, drug-eluting is a medical device that received FDA 510(k) clearance on 2026-03-25. The listed applicant is Cook Ireland, Ltd..
When did Stent, superficial femoral artery, drug-eluting receive FDA 510(k) clearance?
The clearance date for Stent, superficial femoral artery, drug-eluting can be found in the official FDA records.
誰是Stent, 淺表股動脈, 药物釋放應用的登記申請人？
FDA 510(k) 記錄將 Cook Ireland, Ltd. 列為申請人。這並不單獨確立設備製造商。
FDA產品代碼為Stent，表淺股動脈，藥物釋放型是什麼？
FDA對Stent, superficial femoral artery, drug-eluting的產品代碼為NIU。
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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