系統，內血管移植物，主动脉瘤治療
PMA 核准號：P020018 · 2026-09-17
廣告
器材摘要
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 2026-09-17. The device is classified under product code MIH. It was reviewed by the CV advisory panel.
常見問題
What is the SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT?
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT is a medical device that received FDA 510(k) clearance on 2026-09-17. The listed applicant is Cook, Inc..
When did SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT receive FDA 510(k) clearance?
The clearance date for SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT can be found in the official FDA records.
誰是SYSTEM、內血管移植物、主动脉瘤治療的登記申請人？
The FDA 510(k) record lists Cook, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？對於SYSTEM、內血管移植物、主动脉瘤治療產品？
FDA產品代碼對於SYSTEM、內血管移植物、主动脉瘤治療為MIH。
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。
廣告