美敦力Confida布雷克克導絲
K 號：K181001 · 2018-05-03
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器材摘要
Medtronic Confida Brecker Guidewire is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Core Valve, LLC. It received FDA 510(k) clearance on 2018-05-03 under 510(k) number K181001. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Medtronic Confida Brecker Guidewire?
Medtronic Confida Brecker Guidewire is a medical device that received FDA 510(k) clearance on 2018-05-03. The listed applicant is Medtronic Core Valve, LLC. The 510(k) number is K181001.
When did Medtronic Confida Brecker Guidewire receive FDA 510(k) clearance?
Medtronic Confida Brecker Guidewire received FDA 510(k) clearance on 2018-05-03, under 510(k) number K181001.
Who is the listed applicant for Medtronic Confida Brecker Guidewire?
The FDA 510(k) record lists Medtronic Core Valve, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medtronic Confida Brecker Guidewire?
The FDA product code for Medtronic Confida Brecker Guidewire is DQX.
相關臨床試驗
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相關器械（代碼：DQX）
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。
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官方來源
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