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FDA 510(k)

FreedomEdge 渗透系統；高流量 SubQ 鋒針組；精準流量管

K 號：K252015 · 2026-01-28

申請人Koru Medical Systems, Inc.
決定日期2026-01-28
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

FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing is the device name listed in this FDA 510(k) record. The listed applicant is Koru Medical Systems, Inc.. It received FDA 510(k) clearance on 2026-01-28 under 510(k) number K252015. 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 FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing?

FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing is a medical device that received FDA 510(k) clearance on 2026-01-28. The listed applicant is Koru Medical Systems, Inc.. The 510(k) number is K252015.

When did FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing receive FDA 510(k) clearance?

FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing received FDA 510(k) clearance on 2026-01-28, under 510(k) number K252015.

Who is the listed applicant for FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing?

The FDA 510(k) record lists Koru Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing?

The FDA product code for FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate Tubing is FRN.

相關臨床試驗

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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。

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