Coronary drug-eluting stent
PMA 核准號：P170030 · 2026-09-24
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器材摘要
Coronary drug-eluting stent is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik AG. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code NIQ. It was reviewed by the CV advisory panel.
常見問題
What is the Coronary drug-eluting stent?
Coronary drug-eluting stent is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Biotronik AG.
When did Coronary drug-eluting stent receive FDA 510(k) clearance?
The clearance date for Coronary drug-eluting stent can be found in the official FDA records.
Who is the listed applicant for Coronary drug-eluting stent?
The FDA 510(k) record lists Biotronik AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Coronary drug-eluting stent?
The FDA product code for Coronary drug-eluting stent is NIQ.
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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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