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eVox System

Firefly Neuroscience, Inc. · Model EVO-002-400-000 · UDI-DI 00867606000304

HCCGWQGWJ Prescription
10
510(k) clearances
59
Adverse events (1 deaths)
4
Recalls
109
Facilities

Description

The eVox System is intended for the acquisition, display, and storage, of electrical activity of a patient’s brain including electroencephalograph (EEG) and event-related potentials (ERP) obtained by placing two or more electrodes on the head to aid in diagnosis The medical system includes the “eVox System” amplifier device, accessories, and a computer (laptop computer or tablet device with internal battery and power cord). The hardware and ancillary components used in conjunction with the eVox System include an EEG cap, the eVox Amplifier, a charging kit (that consists of a USB cable, clip kit, and wall adapter), a Subject Response Device and a Base Station laptop computer. The software on the Base Station laptop computer is intended for device functioning

Recalls

DateFirmReason
2023-12-11RONAN MEDICAL LLCNeurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.
2017-07-07Ondamed IncThe firm was marketing the Ondamed System in the US without marketing clearance. As a corrective action, the firm revised its device design to comply with regulations. The firm has
2015-10-01Powers Medical Devices, LLCPAL unit has undergone significant technological changes since the previous 510(k) and labeling is not consistent with the cleared indications of the 510(k).
2012-11-15EEG InfoEEG Info, Inc. is recalling the EEG Neuroamp device because they have identified a potential risk associated with the mislabeling of certain devices.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.