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

BrainScope One

K Number: K181179 · Decision May 18, 2018
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
8
Applicant Total
8
Review Days
16

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Basic Information

Device Name
BrainScope One
K Number
K181179
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.1450
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Brainscope Company, Inc.
Date Received
May 2, 2018
Decision Date
May 18, 2018
Product Code
PIW
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
PIW Brain Injury Adjunctive Interpretive Electroencephalograph Assessment Aid

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PIW), ordered by most recent decision date.

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Other Clearances by Brainscope Company, Inc.

K Number Device Name
K190815 BrainScope TBI
K183241 BrainScope TBI (Model: Ahead 400)
K181785 Modified BrainScope One
K161068 Ahead 300
K143643 Brainscope Ahead 200
DEN140025 BrainScope Ahead 100
K082886 ZOOM-100DC