GESCO PER-Q-CATH CATHETER INTRODUCER

GESCO PER-Q-CATH CATHETER INTRODUCER is an FDA 510(k)-cleared medical device (K915167) manufactured by Gesco Intl., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 26, 1992. Regulation: 8.