FDA 510(k)

iiSure 靜脈輸注套件

K 號：K261530 · 2026-06-03

決定日期2026-06-03

產品代碼FPA

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

iiSure Infusion Set is the device name listed in this FDA 510(k) record. The listed applicant is Deka Research and Development. It received FDA 510(k) clearance on 2026-06-03 under 510(k) number K261530. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the iiSure Infusion Set?

iiSure Infusion Set is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Deka Research and Development. The 510(k) number is K261530.

When did iiSure Infusion Set receive FDA 510(k) clearance?

iiSure Infusion Set received FDA 510(k) clearance on 2026-06-03, under 510(k) number K261530.

Who is the listed applicant for iiSure Infusion Set?

The FDA 510(k) record lists Deka Research and Development as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for iiSure Infusion Set?

The FDA product code for iiSure Infusion Set is FPA.

其他以 Deka Research and Development 為申請人之記錄

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相關器械（代碼：FPA）

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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官方來源

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