急性冠狀動脈綜合症事件偵測器
PMA 核准號：P150009 · 2024-08-14
廣告
器材摘要
Acute coronary syndrome event detector is the device name listed in this FDA 510(k) record. The listed applicant is Avertix Medical, Inc.. It received FDA 510(k) clearance on 2024-08-14. The device is classified under product code QBI. It was reviewed by the CV advisory panel.
常見問題
What is the Acute coronary syndrome event detector?
Acute coronary syndrome event detector is a medical device that received FDA 510(k) clearance on 2024-08-14. The listed applicant is Avertix Medical, Inc..
When did Acute coronary syndrome event detector receive FDA 510(k) clearance?
The clearance date for Acute coronary syndrome event detector can be found in the official FDA records.
Who is the listed applicant for Acute coronary syndrome event detector?
The FDA 510(k) record lists Avertix Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Acute coronary syndrome event detector?
The FDA product code for Acute coronary syndrome event detector is QBI.
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。
廣告