NEXUS NIS-6P LUER ACTIVATED DEVICE

NEXUS NIS-6P LUER ACTIVATED DEVICE is an FDA 510(k)-cleared medical device (K133351) manufactured by Nexus Medical, LLC. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 2014. Regulation: 8.