FDA 510(k), K210805, Ceribell Instant EEG Headband

FDA 510(k), K210805, Ceribell Instant EEG Headband

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510(K) Number: K210805
Device Name: Ceribell Instant EEG Headband
Manufacturer: Ceribell, Inc.
Device Classification Name: Electrode, Cutaneous
Regulation Number: 882.1320
Classification Product Code: GXY
Date Received: 03/17/2021
Decision Date: 08/30/2021
Regulation Medical Specialty: Neurology

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