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FDA 510(k)

BD PhaSeal™ Optima 連接組 (C83-O);BD PhaSeal™ Optima 尖嘴組 (C180-O)

K 號:K250059 · 2025-09-12

決定日期2025-09-12
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

BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O) is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2025-09-12 under 510(k) number K250059. 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 BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O)?

BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O) is a medical device that received FDA 510(k) clearance on 2025-09-12. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K250059.

When did BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O) receive FDA 510(k) clearance?

BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O) received FDA 510(k) clearance on 2025-09-12, under 510(k) number K250059.

Who is the listed applicant for BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O)?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O)?

The FDA product code for BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O) is ONB.

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其他以 Becton, Dickinson and Company 為申請人之記錄

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相關器械(代碼:ONB)

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官方來源

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