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.

Creagh Medical, Ltd.

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

Total Devices3
Categories1
Latest Approval2023-03-22
TypeNumberDevice NameCodeDate
510(k) K230191 Arise™ UHP Dilatation Catheter LIT 2023-03-22 View
510(k) K200700 Surmodics Sublime Radial Access 014 RX PTA (Percutaneous Transluminal Angioplasty) Dilatation Catheter LIT 2020-05-14 View
510(k) K180007 018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter LIT 2018-04-19 View