VersaCross™ 電波針
K 號：K242076 · 2024-11-01
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器材摘要
VersaCross™ RF Wire is the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Company. It received FDA 510(k) clearance on 2024-11-01 under 510(k) number K242076. The device is classified under product code DXF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the VersaCross™ RF Wire?
VersaCross™ RF Wire is a medical device that received FDA 510(k) clearance on 2024-11-01. The listed applicant is Baylis Medical Company. The 510(k) number is K242076.
When did VersaCross™ RF Wire receive FDA 510(k) clearance?
VersaCross™ RF Wire received FDA 510(k) clearance on 2024-11-01, under 510(k) number K242076.
Who is the listed applicant for VersaCross™ RF Wire?
The FDA 510(k) record lists Baylis Medical Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VersaCross™ RF Wire?
The FDA product code for VersaCross™ RF Wire is DXF.
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。
相關器械（代碼：DXF）
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
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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