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

EVOPORT 100

K Number: K863985 · Decision Jan 29, 1987
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
75
Applicant Total
92
Review Days
107

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Basic Information

Device Name
EVOPORT 100
K Number
K863985
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1900
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Jedmed Instrument Co.
Date Received
October 14, 1986
Decision Date
January 29, 1987
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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K950925 JEDMED LARYNGEAL SCOPE
K953457 JEDMED SPECTRUM ENT CABINET
K950785 HORTMANN AIRMATIC AIR CALORIC STIMULATOR
K950078 MICROFLOW IRRIGATION SYSTEM
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K944031 VIDEO SCOPE SYSTEM (OTOSCOPE)
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