TRELLIS-8 PERIPHERAL INFUSION SYSTEM

TRELLIS-8 PERIPHERAL INFUSION SYSTEM is an FDA 510(k)-cleared medical device (K130904) manufactured by Covidien. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 24, 2013. Regulation: 8.