分流器，門腔系統，內支架
PMA 核准號：P040027 · 2025-10-27
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器材摘要
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Gore & Associates, Inc.. It received FDA 510(k) clearance on 2025-10-27. The device is classified under product code MIR. It was reviewed by the CV advisory panel.
常見問題
What is the SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS?
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 2025-10-27. The listed applicant is W. L. Gore & Associates, Inc..
When did SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS receive FDA 510(k) clearance?
The clearance date for SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS can be found in the official FDA records.
誰是SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS的登記申請人？
The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
什麼是SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS的FDA產品編碼？
FDA產品代碼為SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS的代碼是MIR。
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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