INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLES

INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLES is an FDA 510(k)-cleared medical device (K131446) manufactured by Integra LifeSciences Corporation. 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 27, 2013. Regulation: 8.