髂蓋覆蓋支架,動脈
PMA 核准號:P160024 · 2025-09-29
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器材摘要
Iliac covered stent, arterial 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 2025-09-29. The device is classified under product code PRL. It was reviewed by the CV advisory panel.
常見問題
What is the Iliac covered stent, arterial?
Iliac covered stent, arterial is a medical device that received FDA 510(k) clearance on 2025-09-29. The listed applicant is Bard Peripheral Vascular, Inc..
When did Iliac covered stent, arterial receive FDA 510(k) clearance?
The clearance date for Iliac covered stent, arterial can be found in the official FDA records.
Who is the listed applicant for Iliac covered stent, arterial?
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。
What is the FDA product code for Iliac covered stent, arterial?
The FDA product code for Iliac covered stent, arterial is PRL.
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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