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

OTE BIOMEDICA NEUROGRAPH 14

K Number: K820603 · Decision Mar 23, 1982
Classifications
1
FEI Numbers
97
Registration Numbers
97
Same Product Code
186
Applicant Total
54
Review Days
18

Basic Information

Device Name
OTE BIOMEDICA NEUROGRAPH 14
K Number
K820603
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
DEL MAR AVIONICS
Date Received
March 5, 1982
Decision Date
March 23, 1982
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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