心臟節律器，單心房，感測驅動，可植入式
PMA 核准號：P850051 · 2025-03-20
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器材摘要
Pulse-generator, single chamber, sensor driven, implantable is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic, Inc.. It received FDA 510(k) clearance on 2025-03-20. The device is classified under product code LWO. It was reviewed by the CV advisory panel.
常見問題
What is the Pulse-generator, single chamber, sensor driven, implantable?
Pulse-generator, single chamber, sensor driven, implantable is a medical device that received FDA 510(k) clearance on 2025-03-20. The listed applicant is Medtronic, Inc..
When did Pulse-generator, single chamber, sensor driven, implantable receive FDA 510(k) clearance?
The clearance date for Pulse-generator, single chamber, sensor driven, implantable can be found in the official FDA records.
誰是 Pulse-generator, single chamber, sensor driven, implantable 的登記申請人？
FDA 510(k) 記錄將美敦力公司（Medtronic, Inc.）列為申請人。這並不單獨確立該設備製造商。
FDA產品代碼為 Pulse-generator, single chamber, sensor driven, implantable 的產品是什麼？
FDA產品代碼，針對心臟節律器，單心房，感測驅動，植入式，為LWO。
相關臨床試驗
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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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