FDA 510(k)

Natus VikingQuest

K-Number: K172743 · 2017-12-19

Decision Date2017-12-19

Product CodeIKN

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing Natus Neurology Incorporated as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243982Nicolet EDX K243495Natus Ultrapro S100 (982A0594)K173366NicoletOne

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K163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.