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  • Zeto’s latest EEG device garners FDA 510(k) clearance for outpatient use

Zeto’s latest EEG device garners FDA 510(k) clearance for outpatient use

  • April 5, 2026

Zeto, which makes brainwave monitors for emergency rooms, received a third FDA clearance for an EEG device. The latest is intended for use in outpatient clinics or at home.

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