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FDA 510(k) Applications Submitted by NEUROSOFT LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K133995
12/26/2013
NEURON-SPECTRUM-4/P WITH NEURON-SPECTRUM.NET SOFTWARE
NEUROSOFT LTD
K190703
03/18/2019
Neuro-IOM system with Neuro-IOM.NET software
Neurosoft Ltd
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