免疫組織化學測試，抗體，程序性死亡配體1
PMA 核准號：P150027 · 2017-03-24
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器材摘要
Immunohistochemistry assay, antibody, programmed death-ligand 1 is the device name listed in this FDA 510(k) record. The listed applicant is Dako North America, Inc.. It received FDA 510(k) clearance on 2017-03-24. The device is classified under product code PLS. It was reviewed by the PA advisory panel.
常見問題
What is the Immunohistochemistry assay, antibody, programmed death-ligand 1?
Immunohistochemistry assay, antibody, programmed death-ligand 1 is a medical device that received FDA 510(k) clearance on 2017-03-24. The listed applicant is Dako North America, Inc..
When did Immunohistochemistry assay, antibody, programmed death-ligand 1 receive FDA 510(k) clearance?
The clearance date for Immunohistochemistry assay, antibody, programmed death-ligand 1 can be found in the official FDA records.
誰是免疫組織化學測試、抗體、程序性死亡配體1的登記申請人？
The FDA 510(k) record lists Dako North America, Inc. as the applicant. This does not by itself establish the device manufacturer.
免疫組織化學測定、抗體、程序性死亡配體1的FDA產品代碼是什麼？
FDA產品代碼為免疫組織化學測試、抗體、程序性死亡配體1的是PLS。
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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