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

Interson Corporation

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

Total Devices2
Categories1
Latest Approval2023-12-22
TypeNumberDevice NameCodeDate
510(k) K233734 Interson USB Ultrasound System IYN 2023-12-22 View
510(k) K163443 Interson USB Ultrasound System IYN 2017-04-13 View