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

MENTOR EEG SYSTEM

K Number: K904763 · Decision Apr 10, 1991
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
48
Review Days
170

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Basic Information

Device Name
MENTOR EEG SYSTEM
K Number
K904763
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Oxford Medilog, Inc.
Date Received
October 22, 1990
Decision Date
April 10, 1991
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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K912639 SONICAID TEAM
K902690 SONICAID MODEL MERIDIAN 800
K895909 SONICAID MODEL VASOFLO 4
K896535 MEDILOG OPTIMA
K891383 MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM
K890330 MEDILOG 6000-FD REPORT GENERATOR
K890338 MEDILOG EDITOR
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