單次使用无菌皮下針頭
K 號:K210232 · 2021-09-23
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器材摘要
常見問題
What is the Sterile Hypodermic Needles for Single Use?
Sterile Hypodermic Needles for Single Use is a medical device that received FDA 510(k) clearance on 2021-09-23. The listed applicant is Zhejiang Kangkang Medical-Devices Co., Ltd.. The 510(k) number is K210232.
When did Sterile Hypodermic Needles for Single Use receive FDA 510(k) clearance?
Sterile Hypodermic Needles for Single Use received FDA 510(k) clearance on 2021-09-23, under 510(k) number K210232.
Who is the listed applicant for Sterile Hypodermic Needles for Single Use?
The FDA 510(k) record lists Zhejiang Kangkang Medical-Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sterile Hypodermic Needles for Single Use?
The FDA product code for Sterile Hypodermic Needles for Single Use is FMI.
相關臨床試驗
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其他以 Zhejiang Kangkang Medical-Devices Co., Ltd. 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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