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.

M3Dicine Pty , Ltd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K193631 Stethee Pro 1, Stethee Pro Software SystemDQD2020-10-09 View
510(k) K172296 Stethee ProDQD2017-10-30 View
↑