GESCO DUAL LUMEN UMBILICATH II-DL

GESCO DUAL LUMEN UMBILICATH II-DL is an FDA 510(k)-cleared medical device (K896041) manufactured by Gesco Intl., Inc.. 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 April 16, 1990. Regulation: 8.