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

MODEL S10VS VISUAL STIMULATOR

K Number: K812061 · Decision Aug 20, 1981
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
48
Applicant Total
6
Review Days
30

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Basic Information

Device Name
MODEL S10VS VISUAL STIMULATOR
K Number
K812061
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Grass Instrument Co.
Date Received
July 21, 1981
Decision Date
August 20, 1981
Product Code
GWE
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
GWE Stimulator, Photic, Evoked Response

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K844216 GRASS MODEL NL FACIAL NERVE LOCATOR & MONITOR
K810539 MODEL S10CTCM AUDITORY STIMULATOR
K771742 EVOKED RESPONSE SYS., MODEL 10