組織膠，用於腦動靜脈畸形栓塞治療
PMA 核准號：P990040 · 2026-05-26
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器材摘要
tissue adhesive for use in embolization of brain arteriovenous malformations is the device name listed in this FDA 510(k) record. The listed applicant is Cerenovus, Inc.. It received FDA 510(k) clearance on 2026-05-26. The device is classified under product code KGG. It was reviewed by the NE advisory panel.
常見問題
What is the tissue adhesive for use in embolization of brain arteriovenous malformations?
tissue adhesive for use in embolization of brain arteriovenous malformations is a medical device that received FDA 510(k) clearance on 2026-05-26. The listed applicant is Cerenovus, Inc..
When did tissue adhesive for use in embolization of brain arteriovenous malformations receive FDA 510(k) clearance?
The clearance date for tissue adhesive for use in embolization of brain arteriovenous malformations can be found in the official FDA records.
Who is the listed applicant for tissue adhesive for use in embolization of brain arteriovenous malformations?
FDA 510(k) 記錄將 Cerenovus, Inc. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for tissue adhesive for use in embolization of brain arteriovenous malformations?
The FDA product code for tissue adhesive for use in embolization of brain arteriovenous malformations is KGG.
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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