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

EES 10 ELECTRODELESS ELECTRICAL STIMULATOR

K Number: K863175 · Decision Jan 13, 1987
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
46
Review Days
148

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Basic Information

Device Name
EES 10 ELECTRODELESS ELECTRICAL STIMULATOR
K Number
K863175
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Cadwell Laboratories, Inc.
Date Received
August 18, 1986
Decision Date
January 13, 1987
Product Code
GWF
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
GWF Stimulator, Electrical, Evoked Response

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K971214 KILOWIN
K962455 FOUR-CHANNEL PREAMPLIFIER
K962457 TWO-CHANNEL PREAMPLIFIER
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K946094 CADWELL EASY AMBULATORY EEG
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