CAPIOX(R) BUBBLE TRAP

CAPIOX(R) BUBBLE TRAP is an FDA 510(k)-cleared medical device (K911632) manufactured by Terumo Medical 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 July 8, 1991. Regulation: 8.