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FDA 510(k)

Chemfort® 28天 20mm 藥瓶適配器及 13mm 轉換器

K 號:K253033 · 2025-10-21

決定日期2025-10-21
產品代碼ONB
諮詢委員會醫療設備規範文本翻譯如下: HO 注意:原文中未提供具體的醫療設備規範文本,因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於

器材摘要

Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor is the device name listed in this FDA 510(k) record. The listed applicant is Simplivia Healthcare , Ltd.. It received FDA 510(k) clearance on 2025-10-21 under 510(k) number K253033. The device is classified under product code ONB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor?

Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor is a medical device that received FDA 510(k) clearance on 2025-10-21. The listed applicant is Simplivia Healthcare , Ltd.. The 510(k) number is K253033.

When did Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor receive FDA 510(k) clearance?

Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor received FDA 510(k) clearance on 2025-10-21, under 510(k) number K253033.

Who is the listed applicant for Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor?

The FDA 510(k) record lists Simplivia Healthcare , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor?

The FDA product code for Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor is ONB.

相關臨床試驗

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其他以 Simplivia Healthcare , 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:ONB)

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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