一次性射頻針管
K 號：K253907 · 2026-04-16
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器材摘要
Disposable Radiofrequency Cannula is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-04-16 under 510(k) number K253907. 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 Radiofrequency Cannula?
Disposable Radiofrequency Cannula is a medical device that received FDA 510(k) clearance on 2026-04-16. The listed applicant is ABBOTT MEDICAL. The 510(k) number is K253907.
When did Disposable Radiofrequency Cannula receive FDA 510(k) clearance?
Disposable Radiofrequency Cannula received FDA 510(k) clearance on 2026-04-16, under 510(k) number K253907.
Who is the listed applicant for Disposable Radiofrequency Cannula?
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 Radiofrequency Cannula?
The FDA product code for Disposable Radiofrequency Cannula is GXI.
相關臨床試驗
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其他以 ABBOTT MEDICAL 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。
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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。
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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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