診斷低電場設備
PMA 核准號：P110014 · 2025-09-17
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決定日期2025-09-17
PMA 編號P110014
產品代碼OEE
器械分類3 類
醫療專科U
諮詢委員會SU
請提供完整的描述文本，以便我進行翻譯。
器材摘要
Diagnostic low electric field is the device name listed in this FDA 510(k) record. The listed applicant is Dilon Medical Technologies, Ltd.. It received FDA 510(k) clearance on 2025-09-17. The device is classified under product code OEE. It was reviewed by the SU advisory panel.
常見問題
What is the Diagnostic low electric field?
Diagnostic low electric field is a medical device that received FDA 510(k) clearance on 2025-09-17. The listed applicant is Dilon Medical Technologies, Ltd..
When did Diagnostic low electric field receive FDA 510(k) clearance?
The clearance date for Diagnostic low electric field can be found in the official FDA records.
Who is the listed applicant for Diagnostic low electric field?
The FDA 510(k) record lists Dilon Medical Technologies, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Diagnostic low electric field?
The FDA product code for Diagnostic low electric field is OEE.
相關臨床試驗
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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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