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FDA 510(k)

神经机器人

K号: K180455 · 2018-05-22

决定日期2018-05-22
产品代码IYN
咨询委员会RA
决定实质等同

器械摘要

NeuralBot is the device name listed in this FDA 510(k) record. The listed applicant is Neural Analytics, Inc.. It received FDA 510(k) clearance on 2018-05-22 under 510(k) number K180455. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the NeuralBot?

NeuralBot is a medical device that received FDA 510(k) clearance on 2018-05-22. The listed applicant is Neural Analytics, Inc.. The 510(k) number is K180455.

When did NeuralBot receive FDA 510(k) clearance?

NeuralBot received FDA 510(k) clearance on 2018-05-22, under 510(k) number K180455.

Who is the listed applicant for NeuralBot?

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

What is the FDA product code for NeuralBot?

The FDA product code for NeuralBot is IYN.

相关临床试验

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列明Neural Analytics, Inc.为申报人的其他记录

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相关器械(代码:IYN)

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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