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FDA 510(k)

VEEGix EEG System

K-Number: K240593 · 2024-08-23

ApplicantNeuroServo, Inc.
Decision Date2024-08-23
Product CodeOLT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VEEGix EEG System is the device name listed in this FDA 510(k) record. The listed applicant is NeuroServo, Inc.. It received FDA 510(k) clearance on 2024-08-23 under 510(k) number K240593. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEEGix EEG System?

VEEGix EEG System is a medical device that received FDA 510(k) clearance on 2024-08-23. The listed applicant is NeuroServo, Inc.. The 510(k) number is K240593.

When did VEEGix EEG System receive FDA 510(k) clearance?

VEEGix EEG System received FDA 510(k) clearance on 2024-08-23, under 510(k) number K240593.

Who is the listed applicant for VEEGix EEG System?

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

What is the FDA product code for VEEGix EEG System?

The FDA product code for VEEGix EEG System is OLT.

Related Devices (Code: OLT)

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.

K253767UB ERP SystemUniversal BrainK251881HippoMind (v1.0)HippoclinicK251366EEG-1260A Neurofax System (EEG-1260A); JE-940A EEG Amplifier Unit (JE-940A); LS-940A Photic Stimulator (LS-940A)Nihon Kohden CorporationK220254Neuron-Spectrum-AM with Neuron-Spectrum.NET SoftwareNeurosoft , Ltd.K213299Wireless EEG SystemPascall Systems, Inc.K191322E-EEGX, N-EEGXGE Healthcare Finland Oy

Official Source

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