Front Line Medical Technologies, Inc. - FDA 510(k) Cleared Devices
1
Total
0
Cleared
0
Denied
Front Line Medical Technologies, Inc. has 0 FDA 510(k) cleared medical devices. Based in London, CA.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Front Line Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Covance as regulatory consultant.
FDA 510(k) Regulatory Record - Front Line Medical Technologies, Inc.
1 devices