510(k) K251381

Device
Ceribell Instant EEG Headcap (Small: C251, Medium: C252)
Applicant
Ceribell, Inc.
510(k) number
K251381
Product code
GXY
Decision
Substantially Equivalent (SESE)
Decision date
2025-10-31
Date received
2025-05-02
Regulation
882.1320
Classification name
Electrode, Cutaneous
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Raymond Woo
Address
360 N. Pastoria Ave. Sunnyvale CA US 94085 94085

FDA Registration Numbers

Source Documents

510(k) summary PDF

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