FDA 510(k)

Natus VikingQuest

K号: K172743 · 2017-12-19

决定日期2017-12-19

产品代码IKN

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决定实质等同

器械摘要

Natus VikingQuest is the device name listed in this FDA 510(k) record. The listed applicant is Natus Neurology Incorporated. It received FDA 510(k) clearance on 2017-12-19 under 510(k) number K172743. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Natus VikingQuest?

Natus VikingQuest is a medical device that received FDA 510(k) clearance on 2017-12-19. The listed applicant is Natus Neurology Incorporated. The 510(k) number is K172743.

When did Natus VikingQuest receive FDA 510(k) clearance?

Natus VikingQuest received FDA 510(k) clearance on 2017-12-19, under 510(k) number K172743.

Who is the listed applicant for Natus VikingQuest?

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

What is the FDA product code for Natus VikingQuest?

The FDA product code for Natus VikingQuest is IKN.

列明Natus Neurology Incorporated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。

K243982Nicolet EDX K243495Natus Ultrapro S100 (982A0594)K173366NicoletOne

官方来源

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