E-Cath STIM 依照崔氏規範
K 號：K202699 · 2020-12-29
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器材摘要
E-Cath STIM acc. Tsui is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2020-12-29 under 510(k) number K202699. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the E-Cath STIM acc. Tsui?
E-Cath STIM acc. Tsui is a medical device that received FDA 510(k) clearance on 2020-12-29. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K202699.
When did E-Cath STIM acc. Tsui receive FDA 510(k) clearance?
E-Cath STIM acc. Tsui received FDA 510(k) clearance on 2020-12-29, under 510(k) number K202699.
Who is the listed applicant for E-Cath STIM acc. Tsui?
The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for E-Cath STIM acc. Tsui?
The FDA product code for E-Cath STIM acc. Tsui is CAZ.
其他以 PAJUNK GmbH Medizintechnologie 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：CAZ）
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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