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FDA 510(k)

MedSource 輸血管路用針頭

K 號:K193278 · 2020-08-07

決定日期2020-08-07
產品代碼FOZ
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

MedSource CathMED IV Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Medsource Labs. It received FDA 510(k) clearance on 2020-08-07 under 510(k) number K193278. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MedSource CathMED IV Catheter?

MedSource CathMED IV Catheter is a medical device that received FDA 510(k) clearance on 2020-08-07. The listed applicant is Medsource Labs. The 510(k) number is K193278.

When did MedSource CathMED IV Catheter receive FDA 510(k) clearance?

MedSource CathMED IV Catheter received FDA 510(k) clearance on 2020-08-07, under 510(k) number K193278.

Who is the listed applicant for MedSource CathMED IV Catheter?

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

What is the FDA product code for MedSource CathMED IV Catheter?

The FDA product code for MedSource CathMED IV Catheter is FOZ.

相關臨床試驗

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相關器械(代碼:FOZ)

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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