CATHETER, CAVA (CAVAFIX)

CATHETER, CAVA (CAVAFIX) is an FDA 510(k)-cleared medical device (K760387) manufactured by B. Braun Instruments. 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 1, 1976. Regulation: 8.