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FDA 510(k)

Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD

K号: K182138 · 2018-09-05

申请人Eleckta Limited
决定日期2018-09-05
产品代码IYE
咨询委员会RA
决定实质等同

器械摘要

Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD is the device name listed in this FDA 510(k) record. The listed applicant is Eleckta Limited. It received FDA 510(k) clearance on 2018-09-05 under 510(k) number K182138. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD?

Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD is a medical device that received FDA 510(k) clearance on 2018-09-05. The listed applicant is Eleckta Limited. The 510(k) number is K182138.

When did Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD receive FDA 510(k) clearance?

Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD received FDA 510(k) clearance on 2018-09-05, under 510(k) number K182138.

Who is the listed applicant for Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD?

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

What is the FDA product code for Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD?

The FDA product code for Precise Treatment System; Synergy platform; Synergy; Infinity; VersaHD is IYE.

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

相关器械（代码：IYE）

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。

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官方来源

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