系統，內血管移植物，動靜脈（AV）透析通路狭窄治療
PMA 核准號：P060002 · 2018-10-11
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器材摘要
System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment is the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular. It received FDA 510(k) clearance on 2018-10-11. The device is classified under product code PFV. It was reviewed by the CV advisory panel.
常見問題
What is the System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment?
System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment is a medical device that received FDA 510(k) clearance on 2018-10-11. The listed applicant is Bard Peripheral Vascular.
When did System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment receive FDA 510(k) clearance?
The clearance date for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment can be found in the official FDA records.
Who is the listed applicant for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment?
The FDA 510(k) record lists Bard Peripheral Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment?
The FDA product code for System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment is PFV.
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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