Pulmonary valve prosthesis percutaneously delivered
PMA 核准號：P200015 · 2026-09-23
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器材摘要
Pulmonary valve prosthesis percutaneously delivered is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Lifesciences, LLC. It received FDA 510(k) clearance on 2026-09-23. The device is classified under product code NPV. It was reviewed by the CV advisory panel.
常見問題
What is the Pulmonary valve prosthesis percutaneously delivered?
Pulmonary valve prosthesis percutaneously delivered is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is Edwards Lifesciences, LLC.
When did Pulmonary valve prosthesis percutaneously delivered receive FDA 510(k) clearance?
The clearance date for Pulmonary valve prosthesis percutaneously delivered can be found in the official FDA records.
Who is the listed applicant for Pulmonary valve prosthesis percutaneously delivered?
The FDA 510(k) record lists Edwards Lifesciences, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pulmonary valve prosthesis percutaneously delivered?
The FDA product code for Pulmonary valve prosthesis percutaneously delivered is NPV.
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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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