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

BRAINSTREAM Disposable Deep Cup EEG Electrodes

K Number: K200540 · Decision Jun 1, 2020
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
82
Review Days
90

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Basic Information

Device Name
BRAINSTREAM Disposable Deep Cup EEG Electrodes
K Number
K200540
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Conmed Corporation
Date Received
March 3, 2020
Decision Date
June 1, 2020
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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