Natus VikingQuest
K-Number: K172743 · 2017-12-19
ApplicantNatus Neurology Incorporated
Decision Date2017-12-19
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Natus VikingQuest is a medical device manufactured by Natus Neurology Incorporated. It received FDA 510(k) clearance on 2017-12-19 under approval 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. It is manufactured by Natus Neurology Incorporated. The 510(k) number is K172743.
When was Natus VikingQuest approved by the FDA?
Natus VikingQuest received FDA 510(k) clearance on 2017-12-19, under approval number K172743.
What company makes Natus VikingQuest?
Natus VikingQuest is manufactured by Natus Neurology Incorporated.
What is the FDA product code for Natus VikingQuest?
The FDA product code for Natus VikingQuest is IKN.
Other Devices by Natus Neurology Incorporated
Related Devices (Code: IKN)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.