ARGYLE NEO-SERT TRIPLE LUMEN UMBILICAL VESSEL CATHETER

ARGYLE NEO-SERT TRIPLE LUMEN UMBILICAL VESSEL CATHETER is an FDA 510(k)-cleared medical device (K951738) manufactured by Sherwood Medical Co.. 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 September 28, 1995. Regulation: 8.