ARROW-GEISS PERCUTANEOUS TPN KIT

ARROW-GEISS PERCUTANEOUS TPN KIT is an FDA 510(k)-cleared medical device (K844080) manufactured by Arrow 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, 1985. Regulation: 8.