系統，內血管移植物，主动脉瘤治療
PMA 核准號：P070016 · 2018-10-10
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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 William Cook Europe Aps. It received FDA 510(k) clearance on 2018-10-10. 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 2018-10-10. The listed applicant is William Cook Europe Aps.
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 William Cook Europe Aps 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。
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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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