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.

Fuji Systems Corp.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K120781 CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTHDQY2012-08-09 View
510(k) K051522 SILBRONCHO DOUBLE LUMEN TUBECBI2005-08-17 View
↑