DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
PMA 核准號：P050023 · 2026-09-25
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器材摘要
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code MRM. It was reviewed by the CV advisory panel.
常見問題
What is the DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER?
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Biotronik, Inc..
When did DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER receive FDA 510(k) clearance?
The clearance date for DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER can be found in the official FDA records.
Who is the listed applicant for DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER?
The FDA 510(k) record lists Biotronik, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER?
The FDA product code for DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER is MRM.
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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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