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FDA 510(k)

Emprint SX消融平台和附件

K号: K171358 · 2017-09-01

申请人Coviden, LLC
决定日期2017-09-01
产品代码NEY
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

Emprint SX Ablation Platform and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Coviden, LLC. It received FDA 510(k) clearance on 2017-09-01 under 510(k) number K171358. The device is classified under product code NEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Emprint SX Ablation Platform and Accessories?

Emprint SX Ablation Platform and Accessories is a medical device that received FDA 510(k) clearance on 2017-09-01. The listed applicant is Coviden, LLC. The 510(k) number is K171358.

When did Emprint SX Ablation Platform and Accessories receive FDA 510(k) clearance?

Emprint SX Ablation Platform and Accessories received FDA 510(k) clearance on 2017-09-01, under 510(k) number K171358.

Who is the listed applicant for Emprint SX Ablation Platform and Accessories?

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

What is the FDA product code for Emprint SX Ablation Platform and Accessories?

The FDA product code for Emprint SX Ablation Platform and Accessories is NEY.

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。

相关器械(代码:NEY)

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

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