SURELIFT PROLAPSE SYSTEM
Jul 2011
282d
Neomedic International has 1 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Neomedic International Filter by specialty or product code using the sidebar.