免疫組織化學測試，抗體，Ki-67
PMA 核准號：P210026 · 2026-09-11
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器材摘要
Immunohistochemistry assay, antibody, Ki-67 is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 2026-09-11. The device is classified under product code QQT. It was reviewed by the PA advisory panel.
常見問題
What is the Immunohistochemistry assay, antibody, Ki-67?
Immunohistochemistry assay, antibody, Ki-67 is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Agilent Technologies, Inc..
When did Immunohistochemistry assay, antibody, Ki-67 receive FDA 510(k) clearance?
The clearance date for Immunohistochemistry assay, antibody, Ki-67 can be found in the official FDA records.
誰是免疫組織化學測試、抗體、Ki-67的登記申請人？
The FDA 510(k) record lists Agilent Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？免疫組織化學測試、抗體、Ki-67？
FDA產品代碼對免疫組織化學測試、抗體、Ki-67為QQT。
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。
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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