藍色尼龍無粉塵病人檢查手套,非無菌
K 號:K210366 · 2021-05-07
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器材摘要
常見問題
What is the Blue Nitrile Powder Free Patient Examination Glove, Non Sterile?
Blue Nitrile Powder Free Patient Examination Glove, Non Sterile is a medical device that received FDA 510(k) clearance on 2021-05-07. The listed applicant is Onetexx Sdn Bhd. The 510(k) number is K210366.
When did Blue Nitrile Powder Free Patient Examination Glove, Non Sterile receive FDA 510(k) clearance?
Blue Nitrile Powder Free Patient Examination Glove, Non Sterile received FDA 510(k) clearance on 2021-05-07, under 510(k) number K210366.
Who is the listed applicant for Blue Nitrile Powder Free Patient Examination Glove, Non Sterile?
The FDA 510(k) record lists Onetexx Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Blue Nitrile Powder Free Patient Examination Glove, Non Sterile?
The FDA product code for Blue 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。
其他以 Onetexx Sdn Bhd 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: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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