PathPresenter 醫療設備規範文本 PathPresenter 醫療影像檢視器
K 號：K250968 · 2025-06-20
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器材摘要
PathPresenter Clinical Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Pathpresenter Corporation. It received FDA 510(k) clearance on 2025-06-20 under 510(k) number K250968. The device is classified under product code QKQ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the PathPresenter Clinical Viewer?
PathPresenter Clinical Viewer is a medical device that received FDA 510(k) clearance on 2025-06-20. The listed applicant is Pathpresenter Corporation. The 510(k) number is K250968.
When did PathPresenter Clinical Viewer receive FDA 510(k) clearance?
PathPresenter Clinical Viewer received FDA 510(k) clearance on 2025-06-20, under 510(k) number K250968.
Who is the listed applicant for PathPresenter Clinical Viewer?
The FDA 510(k) record lists Pathpresenter Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PathPresenter Clinical Viewer?
The FDA product code for PathPresenter Clinical Viewer is QKQ.
相關臨床試驗
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相關器械（代碼：QKQ）
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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