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.

Cathworks, Ltd.

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

Total Devices2
Categories1
Latest FDA decision2019-12-09
TypeNumberDevice NameCodeDateActions
510(k) K192442 FFRangioQEK2019-12-09 View
510(k) K182149 FFRangio SystemQEK2018-12-19 View

Related Clinical Trials

NCT06710210Hybrid Percutaneous Coronary Intervention Combining a Bioresorbable Scaffold With Drug-coated Balloons Versus a Conventional Drug-eluting Stent-based Strategy in Patients With Long and Diffuse Coronary Artery DiseaseRECRUITING
↑