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FDA 510(k)

Veloxion控制器套件，Veloxion流体控制系统，Veloxion切除镜，Veloxion视频控制系统，Veloxion滚筒支架，废物管理管路，组织收集器，废物管理袋

K号: K191341 · 2019-06-13

申请人Corinth Medtech, Inc.
决定日期2019-06-13
产品代码FJL
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

Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags is the device name listed in this FDA 510(k) record. The listed applicant is Corinth Medtech, Inc.. It received FDA 510(k) clearance on 2019-06-13 under 510(k) number K191341. The device is classified under product code FJL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags?

Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags is a medical device that received FDA 510(k) clearance on 2019-06-13. The listed applicant is Corinth Medtech, Inc.. The 510(k) number is K191341.

When did Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags receive FDA 510(k) clearance?

Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags received FDA 510(k) clearance on 2019-06-13, under 510(k) number K191341.

Who is the listed applicant for Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags?

The FDA 510(k) record lists Corinth Medtech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags?

The FDA product code for Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags is FJL.

相关临床试验

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Corinth Medtech, Inc.为申报人的其他记录

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。

K230205Veloxion系统K191335Veloxion控制器套件，Veloxion流体控制系统，Veloxion切除镜，Veloxion视频控制系统，Veloxion滚筒支架，废物管理管路，组织收集器，废物管理袋K190113Veloxion控制器套件，Veloxion流体控制系统，Veloxion切除镜，Veloxion视频控制系统，Veloxion滚筒支架，废物管理管路，组织收集器，废物管理袋K190099Veloxion控制器套件，Veloxion流体控制套件，Veloxion切除镜，Veloxion视频控制单元，Veloxion滚筒架，废物管理管路，组织收集器K180752Veloxion系统，Veloxion控制器套件，Veloxion切除设备套件，Veloxion流体控制系统，Veloxion盐水杆K162979Veloxion系统

查看所有 7 个设备 →

相关器械（代码：FJL）

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。

K232486KARL STORZ单极电切镜带高频电缆Karl Storz SE & CO. KGK221893KARL STORZ 双极切除镜带高频电缆Karl Storz Endoscopy America, Inc.K230205Veloxion系统Corinth Medtech, Inc.K190099Veloxion控制器套件，Veloxion流体控制套件，Veloxion切除镜，Veloxion视频控制单元，Veloxion滚筒架，废物管理管路，组织收集器Corinth Medtech, Inc.K162979Veloxion系统Corinth Medtech, Inc.

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。

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