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FDA 510(k)

貝倫快速輸液器,RI-2(快速輸液器RI-2,每分鐘1000毫升);貝倫快速輸液器,RI-2(快速輸液器RI-2,每分鐘750毫升)

K 號:K242735 · 2024-12-23

決定日期2024-12-23
產品代碼FRN
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

Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min) is the device name listed in this FDA 510(k) record. The listed applicant is Belmont Medical Technologies. It received FDA 510(k) clearance on 2024-12-23 under 510(k) number K242735. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min)?

Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min) is a medical device that received FDA 510(k) clearance on 2024-12-23. The listed applicant is Belmont Medical Technologies. The 510(k) number is K242735.

When did Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min) receive FDA 510(k) clearance?

Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min) received FDA 510(k) clearance on 2024-12-23, under 510(k) number K242735.

Who is the listed applicant for Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min)?

The FDA 510(k) record lists Belmont Medical Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min)?

The FDA product code for Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 1000 ml/min); Belmont Rapid Infuser, RI-2 (Rapid Infuser RI-2, 750 ml/min) is FRN.

相關臨床試驗

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相關器械(代碼:FRN)

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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