Ceribell Pocket EEG Device— 510(k) K170363

Substantially Equivalent

Ceribell, Inc.

FDA 510(k) clearance K170363 for Ceribell Pocket EEG Device, Substantially Equivalent on 2017-05-08. Applicant: Ceribell, Inc..

Clearance details

Applicant: Ceribell, Inc.
Product code: Code OMC
Advisory panel: Neurology
Date received: 2017-02-06
Decision date: 2017-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountainview, CA, US

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