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Galvanic Skin Response Sensor (NB-GSR)

Mind Media Europe B.V. · Model 1.0 · UDI-DI 08719481550073

HCC
10
510(k) clearances
59
Adverse events (1 deaths)
4
Recalls
108
Facilities

Description

NB-GSR: The GSR sensor provides a measure of skin resistance or skin conductance when connected to a NeXus signal acquisition device, which is influenced by the autonomic activation of sweat glands in the skin. The sensor output is not intended to be used for vital monitoring purposes. The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.

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.