FDA 510(k)

Discovery 24

K-Number: K150498 · 2016-01-26

Decision Date2016-01-26

Product CodeGWQ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Discovery 24 is the device name listed in this FDA 510(k) record. The listed applicant is Brainmaster Technologies, Inc.. It received FDA 510(k) clearance on 2016-01-26 under 510(k) number K150498. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Discovery 24?

Discovery 24 is a medical device that received FDA 510(k) clearance on 2016-01-26. The listed applicant is Brainmaster Technologies, Inc.. The 510(k) number is K150498.

When did Discovery 24 receive FDA 510(k) clearance?

Discovery 24 received FDA 510(k) clearance on 2016-01-26, under 510(k) number K150498.

Who is the listed applicant for Discovery 24?

The FDA 510(k) record lists Brainmaster Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Discovery 24?

The FDA product code for Discovery 24 is GWQ.

Other records listing Brainmaster Technologies, 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.

K171414qEEG-Pro

Related Devices (Code: GWQ)

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity Sas K221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, Inc.

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.