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DataLITE LE230 Wireless EMG Sensor

BIOMETRICS LIMITED · Model LE230 · UDI-DI 05060481690638

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

Description

The DataLITE wireless surface EMG sensor gives superb quality of signal and ease of use. With a bandwidth of 5-495 Hz and a built in 1000 gain amplifier and wireless transmitter, surface EMG signals are collected and sent to the Biometrics software for analysis. EMG data can be synchronized real-time with other sensors as part of a complete DataLITE system.This product is independently tested and certified to BS EN 60601-1:2006 + A1:2013

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.