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.

Pulsion Medical Systems SE

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest Approval2020-04-30
TypeNumberDevice NameCodeDate
510(k) K192169 PulsioFlex Monitoring System with ProAQT Sensor DXG 2020-04-30 View
510(k) K171620 PiCCO Catheter KRB 2018-02-21 View
510(k) K172259 PulsioFlex Monitoring System DXG 2018-01-18 View
↑