TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.

TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH. is an FDA 510(k)-cleared medical device (K921856) manufactured by Schneider Intl., Ltd.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 20, 1992. Regulation: 8.