Medico USA, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Medico USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medico USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Provision Consulting Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Medico USA, Inc.
1 devices