無線心臟再同步治療 (CRT)
PMA 核准號：P240028 · 2026-03-27
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器材摘要
Leadless Cardiac Resynchronization Therapy (CRT) is the device name listed in this FDA 510(k) record. The listed applicant is EBR Systems, Inc.. It received FDA 510(k) clearance on 2026-03-27. The device is classified under product code SEG. It was reviewed by the CV advisory panel.
常見問題
What is the Leadless Cardiac Resynchronization Therapy (CRT)?
Leadless Cardiac Resynchronization Therapy (CRT) is a medical device that received FDA 510(k) clearance on 2026-03-27. The listed applicant is EBR Systems, Inc..
When did Leadless Cardiac Resynchronization Therapy (CRT) receive FDA 510(k) clearance?
The clearance date for Leadless Cardiac Resynchronization Therapy (CRT) can be found in the official FDA records.
Who is the listed applicant for Leadless Cardiac Resynchronization Therapy (CRT)?
The FDA 510(k) record lists EBR Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Leadless Cardiac Resynchronization Therapy (CRT)?
The FDA product code for Leadless Cardiac Resynchronization Therapy (CRT) is SEG.
相關臨床試驗
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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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