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FDA 510(k)

Discovery 24

K-Number: K150498 · 2016-01-26

ApplicantBrainmaster Technologies, Inc.
Decision Date2016-01-26
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Discovery 24 is a medical device manufactured by Brainmaster Technologies, Inc.. It received FDA 510(k) clearance on 2016-01-26 under approval 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. It is manufactured by Brainmaster Technologies, Inc.. The 510(k) number is K150498.

When was Discovery 24 approved by the FDA?

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

What company makes Discovery 24?

Discovery 24 is manufactured by Brainmaster Technologies, Inc..

What is the FDA product code for Discovery 24?

The FDA product code for Discovery 24 is GWQ.

Other Devices by Brainmaster Technologies, Inc.

K171414qEEG-Pro

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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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