心臟瓣膜，非同種組織
PMA 核准號：P060038 · 2019-11-21
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器材摘要
heart-valve, non-allograft tissue is the device name listed in this FDA 510(k) record. The listed applicant is Corcym Canada Corp. It received FDA 510(k) clearance on 2019-11-21. The device is classified under product code LWR. It was reviewed by the CV advisory panel.
常見問題
What is the heart-valve, non-allograft tissue?
heart-valve, non-allograft tissue is a medical device that received FDA 510(k) clearance on 2019-11-21. The listed applicant is Corcym Canada Corp.
When did heart-valve, non-allograft tissue receive FDA 510(k) clearance?
The clearance date for heart-valve, non-allograft tissue can be found in the official FDA records.
誰是心臟瓣膜、非同種組織的登記申請人？
The FDA 510(k) record lists Corcym Canada Corp as the applicant. This does not by itself establish the device manufacturer.
FDA心臟瓣膜非同種組織產品代碼是什麼？
FDA對心臟瓣膜、非同種組織產品編碼為LWR。
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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