FDA 510(k) Applications Submitted by NORDICNEUROLAB

FDA 510(k) Number Submission Date Device Name Applicant
K092253 07/28/2009 MODIFICATION TO FMRI HARDWARE SYSTEM NORDICNEUROLAB
K140956 04/14/2014 LCD MONITOR NORDICNEUROLAB
K123306 10/24/2012 NORDIC TUMOREX NORDICNEUROLAB
K133910 12/23/2013 NORDICBRAINEX NORDICNEUROLAB
K073099 11/02/2007 FMRI HARDWARE SYSTEM NORDICNEUROLAB
K080515 02/25/2008 FMRI HARDWARE SYSTEM NORDICNEUROLAB


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