VENOUS M/A INTERNAL JUGULAR KIT

VENOUS M/A INTERNAL JUGULAR KIT is an FDA 510(k)-cleared medical device (K800620) manufactured by Norton Performance Plastics 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 April 23, 1980. Regulation: 8.