支架，下腔静脈
PMA 核准號：P250017 · 2026-04-30
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器材摘要
Stent, vena cava 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 2026-04-30. The device is classified under product code QTL. It was reviewed by the CV advisory panel.
常見問題
What is the Stent, vena cava?
Stent, vena cava is a medical device that received FDA 510(k) clearance on 2026-04-30. The listed applicant is W. L. Gore & Associates, Inc..
When did Stent, vena cava receive FDA 510(k) clearance?
The clearance date for Stent, vena cava can be found in the official FDA records.
Who is the listed applicant for Stent, vena cava?
The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stent, vena cava?
The FDA product code for Stent, vena cava is QTL.
相關臨床試驗
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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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