栓塞劑，血管
PMA 核准號：P250003 · 2026-09-03
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器材摘要
Embolization Agent, Vascular is the device name listed in this FDA 510(k) record. The listed applicant is Instylla, Inc.. It received FDA 510(k) clearance on 2026-09-03. The device is classified under product code QVG. It was reviewed by the CV advisory panel.
常見問題
What is the Embolization Agent, Vascular?
Embolization Agent, Vascular is a medical device that received FDA 510(k) clearance on 2026-09-03. The listed applicant is Instylla, Inc..
When did Embolization Agent, Vascular receive FDA 510(k) clearance?
The clearance date for Embolization Agent, Vascular can be found in the official FDA records.
誰是血管栓塞劑的登記申請人？
The FDA 510(k) record lists Instylla, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？血管栓塞劑？
FDA產品代碼對於栓塞劑、血管類產品為QVG。
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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