單極電極外科器械
K 號：K230650 · 2023-10-12
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器材摘要
Monopolar Electrode Surgical Instrument is the device name listed in this FDA 510(k) record. The listed applicant is Vhmed (Nantong) Co. , Ltd.. It received FDA 510(k) clearance on 2023-10-12 under 510(k) number K230650. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Monopolar Electrode Surgical Instrument?
Monopolar Electrode Surgical Instrument is a medical device that received FDA 510(k) clearance on 2023-10-12. The listed applicant is Vhmed (Nantong) Co. , Ltd.. The 510(k) number is K230650.
When did Monopolar Electrode Surgical Instrument receive FDA 510(k) clearance?
Monopolar Electrode Surgical Instrument received FDA 510(k) clearance on 2023-10-12, under 510(k) number K230650.
Who is the listed applicant for Monopolar Electrode Surgical Instrument?
The FDA 510(k) record lists Vhmed (Nantong) Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Monopolar Electrode Surgical Instrument?
The FDA product code for Monopolar Electrode Surgical Instrument is GEI.
相關臨床試驗
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相關器械（代碼：GEI）
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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