無粉乳膠檢查手套,非无菌
K 號:K221877 · 2022-07-23
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器材摘要
常見問題
What is the Powder-Free Nitrile Examination Glove, Non-Sterile?
Powder-Free Nitrile Examination Glove, Non-Sterile is a medical device that received FDA 510(k) clearance on 2022-07-23. The listed applicant is Goodgloves Industries Sdn Bhd. The 510(k) number is K221877.
When did Powder-Free Nitrile Examination Glove, Non-Sterile receive FDA 510(k) clearance?
Powder-Free Nitrile Examination Glove, Non-Sterile received FDA 510(k) clearance on 2022-07-23, under 510(k) number K221877.
Who is the listed applicant for Powder-Free Nitrile Examination Glove, Non-Sterile?
The FDA 510(k) record lists Goodgloves Industries Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Powder-Free Nitrile Examination Glove, Non-Sterile?
The FDA product code for Powder-Free Nitrile Examination Glove, Non-Sterile is LZA.
相關臨床試驗
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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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