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FDA 510(k), K170363, Ceribell Pocket EEG Device
FDA 510(k), K170363, Ceribell Pocket EEG Device
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$149.00 USD
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510(K) Number: K170363
Device Name: Ceribell Pocket EEG Device
Manufacturer: Ceribell, Inc.
Device Classification Name: reduced- montage standard electroencephalograph
Regulation Number: 882.1400
Classification Product Code: OMC
Date Received: 02/06/2017
Decision Date: 05/08/2017
Regulation Medical Specialty: Neurology
Device Name: Ceribell Pocket EEG Device
Manufacturer: Ceribell, Inc.
Device Classification Name: reduced- montage standard electroencephalograph
Regulation Number: 882.1400
Classification Product Code: OMC
Date Received: 02/06/2017
Decision Date: 05/08/2017
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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