ARROW PERCUTANEOUS SHEATH INTRODUCER KIT AK-07903

ARROW PERCUTANEOUS SHEATH INTRODUCER KIT AK-07903 is an FDA 510(k)-cleared medical device (K940079) manufactured by Arrow 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 November 29, 1994. Regulation: 8.