NIPRO CORELESS NEEDLE/CORELESS NEEDLE SET

NIPRO CORELESS NEEDLE/CORELESS NEEDLE SET is an FDA 510(k)-cleared medical device (K971582) manufactured by Nipro Medical Corp.. 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 December 21, 1997. Regulation: 8.