FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

Okti

K Number: K230073 · Decision Feb 9, 2023
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
9
Review Days
30

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Basic Information

Device Name
Okti
K Number
K230073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Compumedics Limited
Date Received
January 10, 2023
Decision Date
February 9, 2023
Product Code
GWQ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWQ Full-Montage Standard Electroencephalograph

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K072201 COMPUMEDICS SOMTE PSG RECORDING SYSTEM
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K003175 COMPUMEDICS SIESTA SYSTEM