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

NEUROMAP WITH NEURO 100

K Number: K002773 · Decision Oct 23, 2000
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
56
Review Days
47

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Basic Information

Device Name
NEUROMAP WITH NEURO 100
K Number
K002773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radionics, Inc.
Date Received
September 6, 2000
Decision Date
October 23, 2000
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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