淋巴節定位系統，用於哨兵針穿刺術過程中
PMA 核准號：P160053 · 2026-05-18
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決定日期2026-05-18
PMA 編號P160053
產品代碼PUV
器械分類3 類
醫療專科U
諮詢委員會SU
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器材摘要
Lymph node location system during sentinel biopsy procedure is the device name listed in this FDA 510(k) record. The listed applicant is Endomagnetics Ltd.,. It received FDA 510(k) clearance on 2026-05-18. The device is classified under product code PUV. It was reviewed by the SU advisory panel.
常見問題
What is the Lymph node location system during sentinel biopsy procedure?
Lymph node location system during sentinel biopsy procedure is a medical device that received FDA 510(k) clearance on 2026-05-18. The listed applicant is Endomagnetics Ltd.,.
When did Lymph node location system during sentinel biopsy procedure receive FDA 510(k) clearance?
The clearance date for Lymph node location system during sentinel biopsy procedure can be found in the official FDA records.
Who is the listed applicant for Lymph node location system during sentinel biopsy procedure?
The FDA 510(k) record lists Endomagnetics Ltd., as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lymph node location system during sentinel biopsy procedure?
The FDA product code for Lymph node location system during sentinel biopsy procedure is PUV.
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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