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

Ceribell Pocket EEG Device

K Number: K170363 · Decision May 8, 2017
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
27
Applicant Total
13
Review Days
91

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Basic Information

Device Name
Ceribell Pocket EEG Device
K Number
K170363
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ceribell, Inc.
Date Received
February 6, 2017
Decision Date
May 8, 2017
Product Code
OMC
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
OMC Reduced- Montage Standard Electroencephalograph

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Other Clearances by Ceribell, Inc.

K Number Device Name
K260363 Ceribell Brain Monitor Headband
K254033 Ceribell Instant EEG Headset
K251936 Ceribell Delirium Monitor System
K252070 Ceribell Infant Seizure Detection Software
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
Search all 13 clearances from Ceribell, Inc. →