FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Neo

K Number: K192889 · Decision Jan 30, 2020
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
15
Applicant Total
8
Review Days
112

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Basic Information

Device Name
Neo
K Number
K192889
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eemagine Medical Imaging Solutions GmbH
Date Received
October 10, 2019
Decision Date
January 30, 2020
Product Code
OMA
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
OMA Amplitude-Integrated Electroencephalograph

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K Number Device Name
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K172312 eego amplifiers
K110223 WAVEGUARD (TM) EEG CAP
K070358 MAXINSIGHT
K051825 COGNITRACE
K002631 ELECTROENCEPHALOGRAPH SOFTWARE EEMAGINE EEG