Breas Medical AB - FDA 510(k) Cleared Devices

Breas Medical AB has 15 FDA 510(k) cleared anesthesiology devices. Based in Molnlycke, Vastra Gotaland, SE.

Latest FDA clearance: May 2025. Active since 2006.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by O'Connell Regulatory Consultants, Inc. and Oconnell Regulatory Consultants, Inc..