MR條件性杯電極，MR條件性Webb電極
K 號：K172503 · 2017-12-01
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器材摘要
常見問題
What is the MR Conditional Cup Electrode, MR Conditional Webb Electrode?
MR Conditional Cup Electrode, MR Conditional Webb Electrode is a medical device that received FDA 510(k) clearance on 2017-12-01. The listed applicant is Rhythmlink International, LLC. The 510(k) number is K172503.
When did MR Conditional Cup Electrode, MR Conditional Webb Electrode receive FDA 510(k) clearance?
MR Conditional Cup Electrode, MR Conditional Webb Electrode received FDA 510(k) clearance on 2017-12-01, under 510(k) number K172503.
Who is the listed applicant for MR Conditional Cup Electrode, MR Conditional Webb Electrode?
The FDA 510(k) record lists Rhythmlink International, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MR Conditional Cup Electrode, MR Conditional Webb Electrode?
The FDA product code for MR Conditional Cup Electrode, MR Conditional Webb Electrode is GXY.
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。
其他以 Rhythmlink International, LLC 為申請人之記錄
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。
相關器械（代碼：GXY）
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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