Bodycap - FDA 510(k) Cleared Devices

Bodycap has 1 FDA 510(k) cleared medical devices. Based in Herouville Saint Clair, FR.

Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Bodycap Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Arazy Group Consultants, Inc. as regulatory consultant.