FDA 510(k)

qEEG-Pro

K-Number: K171414 · 2018-07-01

Decision Date2018-07-01

Product CodeOLU

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

qEEG-Pro 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 2018-07-01 under 510(k) number K171414. The device is classified under product code OLU. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the qEEG-Pro?

qEEG-Pro is a medical device that received FDA 510(k) clearance on 2018-07-01. The listed applicant is Brainmaster Technologies, Inc.. The 510(k) number is K171414.

When did qEEG-Pro receive FDA 510(k) clearance?

qEEG-Pro received FDA 510(k) clearance on 2018-07-01, under 510(k) number K171414.

Who is the listed applicant for qEEG-Pro?

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 qEEG-Pro?

The FDA product code for qEEG-Pro is OLU.

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.

K150498Discovery 24

Related Devices (Code: OLU)

K253015Cognitive Function Neuroimaging (cfNI) Software (1.0.0)VoxNeuro, Inc.K240420NeuroField Analysis SuiteNeurofield, Inc.K222838iSyncBrain©-CiMediSync, Inc.K212684BrainView QEEG SoftwareMedeia, Inc.K202588BNA PlatformElminda, Ltd.K191432cortiQ PROG.Tec Medical Engineering GmbH

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.