qEEG-Pro
K-Number: K171414 · 2018-07-01
ApplicantBrainmaster Technologies, Inc.
Decision Date2018-07-01
Product CodeOLU
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
qEEG-Pro is a medical device manufactured by Brainmaster Technologies, Inc.. It received FDA 510(k) clearance on 2018-07-01 under approval 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. It is manufactured by Brainmaster Technologies, Inc.. The 510(k) number is K171414.
When was qEEG-Pro approved by the FDA?
qEEG-Pro received FDA 510(k) clearance on 2018-07-01, under approval number K171414.
What company makes qEEG-Pro?
qEEG-Pro is manufactured by Brainmaster Technologies, Inc..
What is the FDA product code for qEEG-Pro?
The FDA product code for qEEG-Pro is OLU.
Other Devices by Brainmaster Technologies, Inc.
Related Devices (Code: OLU)
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.