FDA 510(k)

Arrow® Nitinol Wire

K 號：K241784 · 2024-09-18

決定日期2024-09-18

產品代碼DQX

諮詢委員會履歷

決定相當於

器材摘要

Arrow® Nitinol Wire is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2024-09-18 under 510(k) number K241784. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Arrow® Nitinol Wire?

Arrow® Nitinol Wire is a medical device that received FDA 510(k) clearance on 2024-09-18. The listed applicant is Teleflex Medical. The 510(k) number is K241784.

When did Arrow® Nitinol Wire receive FDA 510(k) clearance?

Arrow® Nitinol Wire received FDA 510(k) clearance on 2024-09-18, under 510(k) number K241784.

Who is the listed applicant for Arrow® Nitinol Wire?

FDA 510(k) 記錄將Teleflex Medical列為申請人。這並不單獨確立設備製造商的身份。

What is the FDA product code for Arrow® Nitinol Wire?

The FDA product code for Arrow® Nitinol Wire is DQX.

其他以 Teleflex Medical 為申請人之記錄

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相關器械（代碼：DQX）

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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