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

TECA VS6 VIDEO STIMULATOR

K Number: K781398 · Decision Aug 23, 1978
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
48
Applicant Total
29
Review Days
8

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Basic Information

Device Name
TECA VS6 VIDEO STIMULATOR
K Number
K781398
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Teca, Inc.
Date Received
August 15, 1978
Decision Date
August 23, 1978
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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K896666 P460, DG32 ELECTROENCEPHALOGRAPH
K894889 TECA NEUROMAPPER 386
K894088 TECA NEUROMAPPER 1620, BRAIN MAPPER
K890881 TECA 1A96, 1A97 AND 1A98 ELECTROENCEPHALOGRAPHS
K884870 TECA/MEDELEC 'CONCEPT' P420
K880593 TECA/MEDELEC MISTRAL
K872931 TECA/MEDELEC TTT THERMAL THRESHOLD TESTER
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