支架，髂靜脈
PMA 核准號：P230021 · 2026-08-26
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決定日期2026-08-26
PMA 編號P230021
產品代碼QAN
器械分類3 類
醫療專科U
諮詢委員會履歷
器材摘要
Stent, iliac vein is the device name listed in this FDA 510(k) record. The listed applicant is Philips Image Guided Therapy Corporation. It received FDA 510(k) clearance on 2026-08-26. The device is classified under product code QAN. It was reviewed by the CV advisory panel.
常見問題
What is the Stent, iliac vein?
Stent, iliac vein is a medical device that received FDA 510(k) clearance on 2026-08-26. The listed applicant is Philips Image Guided Therapy Corporation.
When did Stent, iliac vein receive FDA 510(k) clearance?
The clearance date for Stent, iliac vein can be found in the official FDA records.
誰是Stent, 髖靜脈的登記申請人？
The FDA 510(k) record lists Philips Image Guided Therapy Corporation as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為Stent, 髖內静脉是什麼？
FDA產品代碼，對於髂靜脈支架為QAN。
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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