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FDA 510(k) Applications Submitted by NeuroWave Systems Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K202621
09/10/2020
NeuroSENSE Monitoring System, Model NS-901
NeuroWave Systems Inc.
K142834
09/30/2014
DiscoverEEG System, Model DE-401
NeuroWave Systems Inc.
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