無粉劑氰膠病人檢查手套,非无菌(橙色)
K 號:K192635 · 2020-01-17
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器材摘要
常見問題
What is the Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange)?
Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange) is a medical device that received FDA 510(k) clearance on 2020-01-17. The listed applicant is Wrp Asia Pacific Sdn. Bhd.. The 510(k) number is K192635.
When did Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange) receive FDA 510(k) clearance?
Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange) received FDA 510(k) clearance on 2020-01-17, under 510(k) number K192635.
Who is the listed applicant for Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange)?
The FDA 510(k) record lists Wrp Asia Pacific Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange)?
The FDA product code for Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange) is LZA.
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其他以 Wrp Asia Pacific 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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