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

ELECTROCONDUCTIVE MEDIA

K Number: K904377 · Decision Nov 15, 1991
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
68
Applicant Total
44
Review Days
417

Basic Information

Device Name
ELECTROCONDUCTIVE MEDIA
K Number
K904377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1275
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
HENLEY INTL.
Date Received
September 24, 1990
Decision Date
November 15, 1991
Product Code
GYB
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
GYB Media, Electroconductive

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