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.

Zurich Medical, Inc.

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest Approval2019-08-14
TypeNumberDevice NameCodeDate
510(k) K190852 Zurich Pressure Guidewire System Model 100 DXO 2019-08-14 View