XOD 電熱療法無線頻率設備
K 號：K242175 · 2025-02-27
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器材摘要
XOD Diathermia Radiofrequency Device is the device name listed in this FDA 510(k) record. The listed applicant is Xod, Inc.. It received FDA 510(k) clearance on 2025-02-27 under 510(k) number K242175. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the XOD Diathermia Radiofrequency Device?
XOD Diathermia Radiofrequency Device is a medical device that received FDA 510(k) clearance on 2025-02-27. The listed applicant is Xod, Inc.. The 510(k) number is K242175.
When did XOD Diathermia Radiofrequency Device receive FDA 510(k) clearance?
XOD Diathermia Radiofrequency Device received FDA 510(k) clearance on 2025-02-27, under 510(k) number K242175.
Who is the listed applicant for XOD Diathermia Radiofrequency Device?
The FDA 510(k) record lists Xod, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XOD Diathermia Radiofrequency Device?
The FDA product code for XOD Diathermia Radiofrequency Device is PBX.
相關臨床試驗
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相關器械（代碼：PBX）
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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