刺激器，頸動脈神經窦
PMA 核准號：P180050 · 2025-07-11
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器材摘要
Stimulator, carotid sinus nerve is the device name listed in this FDA 510(k) record. The listed applicant is Cvrx, Inc.. It received FDA 510(k) clearance on 2025-07-11. The device is classified under product code DSR. It was reviewed by the CV advisory panel.
常見問題
What is the Stimulator, carotid sinus nerve?
Stimulator, carotid sinus nerve is a medical device that received FDA 510(k) clearance on 2025-07-11. The listed applicant is Cvrx, Inc..
When did Stimulator, carotid sinus nerve receive FDA 510(k) clearance?
The clearance date for Stimulator, carotid sinus nerve can be found in the official FDA records.
Who is the listed applicant for Stimulator, carotid sinus nerve?
The FDA 510(k) record lists Cvrx, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, carotid sinus nerve?
The FDA product code for Stimulator, carotid sinus nerve is DSR.
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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