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

MAXINSIGHT

K Number: K070358 · Decision Jul 30, 2007
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
23
Applicant Total
8
Review Days
173

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Basic Information

Device Name
MAXINSIGHT
K Number
K070358
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
February 7, 2007
Decision Date
July 30, 2007
Product Code
OLX
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
OLX Source Localization Software For Electroencephalograph Or Magnetoencephalograph

Similar 510(k) Clearances

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Other Clearances by Eemagine Medical Imaging Solutions GmbH

K Number Device Name
K240575 WaveGuard Net EEG Cap (NA-245, NA-255, NA-261, NA-265, NA-271, NA-281)
K210109 visor2 system
K192889 Neo
K172312 eego amplifiers
K110223 WAVEGUARD (TM) EEG CAP
K051825 COGNITRACE
K002631 ELECTROENCEPHALOGRAPH SOFTWARE EEMAGINE EEG