Transvenous temporary phrenic nerve stimulator
PMA 核准號：P240012 · 2026-09-25
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器材摘要
Transvenous temporary phrenic nerve stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Lungpacer Medical USA, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code SDL. It was reviewed by the AN advisory panel.
常見問題
What is the Transvenous temporary phrenic nerve stimulator?
Transvenous temporary phrenic nerve stimulator is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Lungpacer Medical USA, Inc..
When did Transvenous temporary phrenic nerve stimulator receive FDA 510(k) clearance?
The clearance date for Transvenous temporary phrenic nerve stimulator can be found in the official FDA records.
Who is the listed applicant for Transvenous temporary phrenic nerve stimulator?
The FDA 510(k) record lists Lungpacer Medical USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Transvenous temporary phrenic nerve stimulator?
The FDA product code for Transvenous temporary phrenic nerve stimulator is SDL.
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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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