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.

Blease USA, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K051629 BLEAS ESIRIUC ANAESTHSIA SYSTEM, MODELS 3000, 2000BSZ2005-09-23 View
510(k) K942799 DATUMCAD1995-04-13 View
↑