FDA 510(k)

C-Lant Port

K 號：K252714 · 2026-02-27

決定日期2026-02-27

產品代碼GCJ

諮詢委員會GU

決定相當於

器材摘要

C-Lant Port is the device name listed in this FDA 510(k) record. The listed applicant is Vigor Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2026-02-27 under 510(k) number K252714. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the C-Lant Port?

C-Lant Port is a medical device that received FDA 510(k) clearance on 2026-02-27. The listed applicant is Vigor Medical Technologies , Ltd.. The 510(k) number is K252714.

When did C-Lant Port receive FDA 510(k) clearance?

C-Lant Port received FDA 510(k) clearance on 2026-02-27, under 510(k) number K252714.

Who is the listed applicant for C-Lant Port?

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

What is the FDA product code for C-Lant Port?

The FDA product code for C-Lant Port is GCJ.

相關器械（代碼：GCJ）

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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