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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