FDA 510(k)

NeuralBot

K-Number: K180455 · 2018-05-22

Decision Date2018-05-22

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing Neural Analytics, Inc. 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.

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Related Devices (Code: IYN)

Official Source

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