IAB-04840-U;IAB-04250-U;IAB-04240-U;IAB-04230-U

IAB-04840-U;IAB-04250-U;IAB-04240-U;IAB-04230-U is an FDA 510(k)-cleared medical device (K970689) 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 June 3, 1998. Regulation: 8.