FDA 510(k) Applications Submitted by NordicNeuroLab AS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K241608	06/04/2024	nordicMEDiVA	NordicNeuroLab AS
K243209	10/01/2024	nordicMEDiVA	NordicNeurolab AS
K191032	04/18/2019	fMRI Hardware System	NordicNeurolab AS
K212720	08/27/2021	nordicDSC	NordicNeurolab AS
K232680	09/01/2023	fMRI Hardware System	NordicNeuroLab AS
K163324	11/25/2016	nordicBrainEx	NordicNeurolab AS