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.

Tokyo Boeki Medisys, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K110520 BIOLIS 12ICEM2012-03-23 View
510(k) K103531 PRESTIGE 24I; BIOLIS 24I; MGC 240CFR2011-12-01 View
↑