PENTAX醫療EPK-i7010影片處理器,配EB系列鏡頭
K 號:K173679 · 2018-07-03
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器材摘要
常見問題
What is the PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?
PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is a medical device that received FDA 510(k) clearance on 2018-07-03. The listed applicant is Pentax of America, Inc.. The 510(k) number is K173679.
When did PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes receive FDA 510(k) clearance?
PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes received FDA 510(k) clearance on 2018-07-03, under 510(k) number K173679.
Who is the listed applicant for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?
The FDA 510(k) record lists Pentax of America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes?
The FDA product code for PENTAX Medical EPK-i7010 Video Processor with EB Family of Scopes is PEA.
相關臨床試驗
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其他以 Pentax of America, Inc. 為申請人之記錄
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。
相關器械(代碼:PEA)
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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