CardioTag™
K 號：K243566 · 2025-07-22
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器材摘要
CardioTag™ is the device name listed in this FDA 510(k) record. The listed applicant is Cardiosense, Inc.. It received FDA 510(k) clearance on 2025-07-22 under 510(k) number K243566. The device is classified under product code DXR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CardioTag™?
CardioTag™ is a medical device that received FDA 510(k) clearance on 2025-07-22. The listed applicant is Cardiosense, Inc.. The 510(k) number is K243566.
When did CardioTag™ receive FDA 510(k) clearance?
CardioTag™ received FDA 510(k) clearance on 2025-07-22, under 510(k) number K243566.
Who is the listed applicant for CardioTag™?
The FDA 510(k) record lists Cardiosense, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CardioTag™?
The FDA product code for CardioTag™ is DXR.
相關臨床試驗
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相關器械（代碼：DXR）
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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