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FDA 510(k) Applications Submitted by NordicNeurolab AS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191032
04/18/2019
fMRI Hardware System
NordicNeurolab AS
K212720
08/27/2021
nordicDSC
NordicNeurolab AS
K163324
11/25/2016
nordicBrainEx
NordicNeurolab AS
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