藥物釋放周邊經皮腔內血管成形術導管
PMA 核准號：P190019 · 2026-08-04
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器材摘要
Drug-Eluting Peripheral Transluminal Angioplasty Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2026-08-04. The device is classified under product code ONU. It was reviewed by the CV advisory panel.
常見問題
What is the Drug-Eluting Peripheral Transluminal Angioplasty Catheter?
Drug-Eluting Peripheral Transluminal Angioplasty Catheter is a medical device that received FDA 510(k) clearance on 2026-08-04. The listed applicant is Boston Scientific Corporation.
When did Drug-Eluting Peripheral Transluminal Angioplasty Catheter receive FDA 510(k) clearance?
The clearance date for Drug-Eluting Peripheral Transluminal Angioplasty Catheter can be found in the official FDA records.
誰是藥物釋放性周邊經皮腔內血管成形術導管的登記申請人？
FDA 510(k) 記錄中將波士頓科學公司列為申請人。這並不單獨確立設備製造商。
FDA產品代碼是什麼？藥物釋放性周邊經皮腔內血管成形術導管？
FDA產品代碼，針對藥物釋放性周邊經皮腔內血管成形術導管為ONU。
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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