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FDA 510(k)

ENFit 至 ENFit 延伸組

K 號:K230326 · 2023-11-02

申請人Vesco Medical
決定日期2023-11-02
產品代碼PIF
諮詢委員會GU
決定相當於

器材摘要

ENFit to ENFit Extension Sets is the device name listed in this FDA 510(k) record. The listed applicant is Vesco Medical. It received FDA 510(k) clearance on 2023-11-02 under 510(k) number K230326. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ENFit to ENFit Extension Sets?

ENFit to ENFit Extension Sets is a medical device that received FDA 510(k) clearance on 2023-11-02. The listed applicant is Vesco Medical. The 510(k) number is K230326.

When did ENFit to ENFit Extension Sets receive FDA 510(k) clearance?

ENFit to ENFit Extension Sets received FDA 510(k) clearance on 2023-11-02, under 510(k) number K230326.

Who is the listed applicant for ENFit to ENFit Extension Sets?

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

What is the FDA product code for ENFit to ENFit Extension Sets?

The FDA product code for ENFit to ENFit Extension Sets is PIF.

相關臨床試驗

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相關器械(代碼:PIF)

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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