FDA 510(k)

DISINTEK™ PA 測試條

K 號：K251035 · 2025-06-03

決定日期2025-06-03

產品代碼JOJ

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

DISINTEK™ PA Test Strips is the device name listed in this FDA 510(k) record. The listed applicant is Serim Research. It received FDA 510(k) clearance on 2025-06-03 under 510(k) number K251035. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the DISINTEK™ PA Test Strips?

DISINTEK™ PA Test Strips is a medical device that received FDA 510(k) clearance on 2025-06-03. The listed applicant is Serim Research. The 510(k) number is K251035.

When did DISINTEK™ PA Test Strips receive FDA 510(k) clearance?

DISINTEK™ PA Test Strips received FDA 510(k) clearance on 2025-06-03, under 510(k) number K251035.

Who is the listed applicant for DISINTEK™ PA Test Strips?

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

What is the FDA product code for DISINTEK™ PA Test Strips?

The FDA product code for DISINTEK™ PA Test Strips is JOJ.

其他以 Serim Research 為申請人之記錄

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相關器械（代碼：JOJ）

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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