皮下針-Pro EDGE 安全設備
K 號:K211634 · 2021-08-26
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器材摘要
常見問題
What is the Hypodermic Needle-Pro EDGE Safety Device?
Hypodermic Needle-Pro EDGE Safety Device is a medical device that received FDA 510(k) clearance on 2021-08-26. The listed applicant is Smiths Medical Asd, Inc.. The 510(k) number is K211634.
When did Hypodermic Needle-Pro EDGE Safety Device receive FDA 510(k) clearance?
Hypodermic Needle-Pro EDGE Safety Device received FDA 510(k) clearance on 2021-08-26, under 510(k) number K211634.
Who is the listed applicant for Hypodermic Needle-Pro EDGE Safety Device?
The FDA 510(k) record lists Smiths Medical Asd, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hypodermic Needle-Pro EDGE Safety Device?
The FDA product code for Hypodermic Needle-Pro EDGE Safety Device is FMI.
相關臨床試驗
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其他以 Smiths Medical Asd, Inc. 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:FMI)
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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