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.

Maquet S.A.S.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130513 VOLISTA 400; VOLISTA 600FTD2013-05-08 View
510(k) K113679 LUCEA LED SURGICAL LIGHT SYSTEMNTN2012-01-12 View
↑