閉塞器，動脈导管，動脈導管閉塞
PMA 核准號：P020024 · 2026-05-28
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器材摘要
OCCLUDER, PATENT DUCTUS, ARTERIOSUS is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-05-28. The device is classified under product code MAE. It was reviewed by the CV advisory panel.
常見問題
What is the OCCLUDER, PATENT DUCTUS, ARTERIOSUS?
OCCLUDER, PATENT DUCTUS, ARTERIOSUS is a medical device that received FDA 510(k) clearance on 2026-05-28. The listed applicant is ABBOTT MEDICAL.
When did OCCLUDER, PATENT DUCTUS, ARTERIOSUS receive FDA 510(k) clearance?
The clearance date for OCCLUDER, PATENT DUCTUS, ARTERIOSUS can be found in the official FDA records.
Who is the listed applicant for OCCLUDER, PATENT DUCTUS, ARTERIOSUS?
The FDA 510(k) record lists ABBOTT MEDICAL as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OCCLUDER, PATENT DUCTUS, ARTERIOSUS?
The FDA product code for OCCLUDER, PATENT DUCTUS, ARTERIOSUS is MAE.
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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