心臟瓣膜，機械式
PMA 核准號：P990046 · 2023-11-07
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器材摘要
HEART-VALVE, MECHANICAL is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Ats Medical, Inc.. It received FDA 510(k) clearance on 2023-11-07. The device is classified under product code LWQ. It was reviewed by the CV advisory panel.
常見問題
What is the HEART-VALVE, MECHANICAL?
HEART-VALVE, MECHANICAL is a medical device that received FDA 510(k) clearance on 2023-11-07. The listed applicant is Medtronic Ats Medical, Inc..
When did HEART-VALVE, MECHANICAL receive FDA 510(k) clearance?
The clearance date for HEART-VALVE, MECHANICAL can be found in the official FDA records.
誰是HEART-VALVE, MECHANICAL的列名申請人？
The FDA 510(k) record lists Medtronic Ats Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為何是HEART-VALVE, MECHANICAL？
FDA產品代碼為HEART-VALVE, MECHANICAL的代碼是LWQ。
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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