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FDA 510(k)

一次性RF電極(RFDE-5/RFDE-10/RFDE-15/RFDE-20)

K 號:K242841 · 2025-05-27

決定日期2025-05-27
產品代碼GXI
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20) is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2025-05-27 under 510(k) number K242841. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)?

Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20) is a medical device that received FDA 510(k) clearance on 2025-05-27. The listed applicant is ABBOTT MEDICAL. The 510(k) number is K242841.

When did Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20) receive FDA 510(k) clearance?

Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20) received FDA 510(k) clearance on 2025-05-27, under 510(k) number K242841.

Who is the listed applicant for Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)?

The FDA 510(k) record lists ABBOTT MEDICAL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)?

The FDA product code for Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20) is GXI.

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 ABBOTT MEDICAL 為申請人之記錄

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相關器械(代碼:GXI)

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

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