Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Neurowave Systems, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K202621 NeuroSENSE Monitoring System, Model NS-901OLW2021-08-05 View
510(k) K092477 NeuroWave NeuroFAST MONITORING SYSTEM, MODEL NF-701OMC2010-10-29 View
↑