THE S. CORDERO STYLUS
Oct 1986
14d
S. Cordero Co. has 1 FDA 510(k) cleared medical devices. Based in Mexico City Cp 01030, MX.
Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by S. Cordero Co. Filter by specialty or product code using the sidebar.