DilaCheck 硅膠無粉檢查手套,(無菌)
K 號:K163035 · 2017-07-07
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器材摘要
常見問題
What is the DilaCheck Nitrile Powder Free Examination Glove, (Sterile)?
DilaCheck Nitrile Powder Free Examination Glove, (Sterile) is a medical device that received FDA 510(k) clearance on 2017-07-07. The listed applicant is Elm Tree Medical, Inc.. The 510(k) number is K163035.
When did DilaCheck Nitrile Powder Free Examination Glove, (Sterile) receive FDA 510(k) clearance?
DilaCheck Nitrile Powder Free Examination Glove, (Sterile) received FDA 510(k) clearance on 2017-07-07, under 510(k) number K163035.
Who is the listed applicant for DilaCheck Nitrile Powder Free Examination Glove, (Sterile)?
The FDA 510(k) record lists Elm Tree Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DilaCheck Nitrile Powder Free Examination Glove, (Sterile)?
The FDA product code for DilaCheck Nitrile Powder Free Examination Glove, (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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