針對股動脈的支架
PMA 核准號：P080007 · 2022-05-26
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器材摘要
STENT, ILIAC is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2022-05-26. The device is classified under product code NIO. It was reviewed by the CV advisory panel.
常見問題
What is the STENT, ILIAC?
STENT, ILIAC is a medical device that received FDA 510(k) clearance on 2022-05-26. The listed applicant is Bard Peripheral Vascular, Inc..
When did STENT, ILIAC receive FDA 510(k) clearance?
The clearance date for STENT, ILIAC can be found in the official FDA records.
誰是STENT, ILIAC的列名申請人？
FDA 510(k) 記錄將 Bard Peripheral Vascular, Inc. 列為申請人。這並不單獨確立設備製造商。
FDA產品代碼為STENT, ILIAC的是什麼？
FDA產品代碼，對於STENT, ILIAC為NIO。
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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