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FDA 510(k)

NeuralBot

K-Number: K180455 · 2018-05-22

ApplicantNeural Analytics, Inc.
Decision Date2018-05-22
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the NeuralBot?

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

When was NeuralBot approved by the FDA?

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

What company makes NeuralBot?

NeuralBot is manufactured by Neural Analytics, Inc..

What is the FDA product code for NeuralBot?

The FDA product code for NeuralBot is IYN.

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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.

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