免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

C-Lant 端口

K号: K252714 · 2026-02-27

决定日期2026-02-27
产品代码GCJ
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定实质等同

器械摘要

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.

常见问题

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.

相关器械(代码:GCJ)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。

↑