FDA 510(k) Applications Submitted by Ceribell, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K170363 02/06/2017 Ceribell Pocket EEG Device Ceribell, Inc.
K191301 05/14/2019 Ceribell Pocket EEG Device Ceribell, Inc.
K171459 05/18/2017 Ceribell Instant EEG Headband Ceribell, Inc.
K210805 03/17/2021 Ceribell Instant EEG Headband Ceribell, Inc.
K232052 07/10/2023 Ceribell Instant EEG Headband Ceribell, Inc.
K223086 09/30/2022 Ceribell Instant EEG Headcap Ceribell, Inc.
K223504 11/22/2022 Ceribell Status Epilepticus Monitor Ceribell, Inc.


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