黑硝基粉末無菌病人檢查手套,非无菌
K 號:K233740 · 2024-02-13
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器材摘要
常見問題
What is the Black Nitrile Powder Free Patient Examination Glove, Non Sterile?
Black Nitrile Powder Free Patient Examination Glove, Non Sterile is a medical device that received FDA 510(k) clearance on 2024-02-13. The listed applicant is W.A. Rubbermate Co., Ltd.. The 510(k) number is K233740.
When did Black Nitrile Powder Free Patient Examination Glove, Non Sterile receive FDA 510(k) clearance?
Black Nitrile Powder Free Patient Examination Glove, Non Sterile received FDA 510(k) clearance on 2024-02-13, under 510(k) number K233740.
Who is the listed applicant for Black Nitrile Powder Free Patient Examination Glove, Non Sterile?
The FDA 510(k) record lists W.A. Rubbermate Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Black Nitrile Powder Free Patient Examination Glove, Non Sterile?
The FDA product code for Black Nitrile Powder Free Patient Examination Glove, Non Sterile is LZA.
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。
相關器械(代碼:LZA)
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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