PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK

PERCUTANEOUS INTROD W/SIDEPORT/THREE-WAY STOPCOCK is an FDA 510(k)-cleared medical device (K910861) manufactured by Daig Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 6, 1991. Regulation: 8.