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

SIGNAL PROCESSOR/AVERAGER MODEL 7S11

K Number: K770878 · Decision Jun 1, 1977
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
8
Review Days
20

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Basic Information

Device Name
SIGNAL PROCESSOR/AVERAGER MODEL 7S11
K Number
K770878
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1900
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Medical Systems Corp.
Date Received
May 12, 1977
Decision Date
June 1, 1977
Product Code
GWJ
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
GWJ Stimulator, Auditory, Evoked Response

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