Medical Industries America, Inc. - FDA 510(k) Cleared Devices

Medical Industries America, Inc. has 19 FDA 510(k) cleared anesthesiology devices. Based in Australia 2038, AU.

Historical record: 19 cleared submissions from 1986 to 2005.

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 Entela, Inc. and Intertek Testing Services.