FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Ceribell Instant EEG Headset

K Number: K254033 · Decision Feb 9, 2026
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
13
Review Days
55

Basic Information

Device Name
Ceribell Instant EEG Headset
K Number
K254033
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ceribell, Inc.
Date Received
December 16, 2025
Decision Date
February 9, 2026
Product Code
GXY
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GXY Electrode, Cutaneous

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K251381 Ceribell Instant EEG Headcap (Small: C251, Medium: C252)
K241589 Ceribell Seizure Detection Software
K232052 Ceribell Instant EEG Headband
K223504 Ceribell Status Epilepticus Monitor
K223086 Ceribell Instant EEG Headcap
K210805 Ceribell Instant EEG Headband
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