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

BRAINET

K Number: K021986 · Decision Aug 23, 2002
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
10
Review Days
66

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Basic Information

Device Name
BRAINET
K Number
K021986
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nicolet Biomedical, Inc.
Date Received
June 18, 2002
Decision Date
August 23, 2002
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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