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.

Medien International Co, Ltd.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K172435 Galaxy R Digital Radiography UpgradeMQB2017-10-13 View
510(k) K093816 DIGITAL RADIOGRAPHY SYSTEM, MODELS GALAXY 900 AND 1600KPR2010-10-05 View
↑