MEADOX SURGIMED OLBERT CATHETER SYSTEM NOPROFILE

MEADOX SURGIMED OLBERT CATHETER SYSTEM NOPROFILE is an FDA 510(k)-cleared medical device (K934411) manufactured by Meadox Medicals, Div. Boston Scientific Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 1994. Regulation: 8.