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

CEREGROTRAC

K Number: K842784 · Decision Jan 10, 1985
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
16
Review Days
177

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Basic Information

Device Name
CEREGROTRAC
K Number
K842784
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Advanced Instruments, Inc.
Date Received
July 17, 1984
Decision Date
January 10, 1985
Product Code
GWQ
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
GWQ Full-Montage Standard Electroencephalograph

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