ClearanceBrief
Company ยท US

Eemagine Medical Imaging Solutions GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2024. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GXYElectrode, Cutaneous2
OLXSource Localization Software For Electroencephalograph Or Magnetoencephalograph2
GWLAmplifier, Physiological Signal1
GWQFull-Montage Standard Electroencephalograph1
HAWNeurological Stereotaxic Instrument1
OMAAmplitude-Integrated Electroencephalograph1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 25, 2024K240575WaveGuard Net EEG Cap (NA-245, NA-255, NA-261, NA-265, NA-271, NA-281)
Eemagine Medical Imaging Solutions GmbH, DE
GXY
Apr 8, 2022K210109visor2 system
Eemagine Medical Imaging Solutions GmbH, DE
HAW
Jan 30, 2020K192889Neo
Eemagine Medical Imaging Solutions GmbH, DE
OMA
Mar 30, 2018K172312eego amplifiers
Eemagine Medical Imaging Solutions GmbH, DE
GWL
Jun 29, 2011K110223WAVEGUARD (TM) EEG CAP
Eemagine Medical Imaging Solutions GmbH
GXY
Jul 30, 2007K070358MAXINSIGHT
Eemagine Medical Imaging Solutions GmbH
OLX
Sep 12, 2005K051825COGNITRACE
Eemagine Medical Imaging Solutions GmbH
GWQ
Oct 23, 2000K002631ELECTROENCEPHALOGRAPH SOFTWARE EEMAGINE EEG
Eemagine Medical Imaging Solutions GmbH
OLX

Latest recalls

DateFirm and productCodeLinked 510(k)
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