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FDA 510(k)

無菌單次使用針頭清潔器(WK800-S10 ,WK800-S20)

K 號:K241022 · 2024-07-11

決定日期2024-07-11
產品代碼GEI
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Sterile single use tip cleaner (WK800-S10 , WK800-S20) is the device name listed in this FDA 510(k) record. The listed applicant is Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. It received FDA 510(k) clearance on 2024-07-11 under 510(k) number K241022. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sterile single use tip cleaner (WK800-S10 , WK800-S20)?

Sterile single use tip cleaner (WK800-S10 , WK800-S20) is a medical device that received FDA 510(k) clearance on 2024-07-11. The listed applicant is Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd. The 510(k) number is K241022.

When did Sterile single use tip cleaner (WK800-S10 , WK800-S20) receive FDA 510(k) clearance?

Sterile single use tip cleaner (WK800-S10 , WK800-S20) received FDA 510(k) clearance on 2024-07-11, under 510(k) number K241022.

Who is the listed applicant for Sterile single use tip cleaner (WK800-S10 , WK800-S20)?

The FDA 510(k) record lists Wickimed (Huizhou) Medical Equipment Manufacturing Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sterile single use tip cleaner (WK800-S10 , WK800-S20)?

The FDA product code for Sterile single use tip cleaner (WK800-S10 , WK800-S20) is GEI.

相關臨床試驗

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其他以 Wickimed (Huizhou) Medical Equipment Manufacturing 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:GEI)

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

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