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.

Noraxon USA, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K895635 MYOSYSTEM 1000 ELECTROMYOGRAPHHCC1990-04-19 View
510(k) K895633 MYOTRACE 10 BIOFEEDBACK DEVICEHCC1990-04-13 View
↑