黑硝基無粉塵病人檢查手套,非無菌
K 號:K220428 · 2022-05-10
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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 2022-05-10. The listed applicant is One Glove Industrial Sdn Bhd. The 510(k) number is K220428.
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 2022-05-10, under 510(k) number K220428.
Who is the listed applicant for Black Nitrile Powder-Free Patient Examination Glove, Non-Sterile?
The FDA 510(k) record lists One Glove Industrial Sdn Bhd 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。
其他以 One Glove Industrial 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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