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FDA 510(k)

K-Pack Embrace 活動安全針 (KNAS-2516RB, KNAS-2525RB)

K 號:K251447 · 2025-07-08

決定日期2025-07-08
產品代碼FMI
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

K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB) is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Europe N.V.. It received FDA 510(k) clearance on 2025-07-08 under 510(k) number K251447. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB)?

K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB) is a medical device that received FDA 510(k) clearance on 2025-07-08. The listed applicant is Terumo Europe N.V.. The 510(k) number is K251447.

When did K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB) receive FDA 510(k) clearance?

K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB) received FDA 510(k) clearance on 2025-07-08, under 510(k) number K251447.

Who is the listed applicant for K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB)?

The FDA 510(k) record lists Terumo Europe N.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB)?

The FDA product code for K-Pack Embrace Active Safety Needle (KNAS-2516RB, KNAS-2525RB) is FMI.

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其他以 Terumo Europe N.V. 為申請人之記錄

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相關器械(代碼:FMI)

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