FILTER (7220&7221 MOBIN-UDDIN VENA CAVA)

FILTER (7220&7221 MOBIN-UDDIN VENA CAVA) is an FDA 510(k)-cleared medical device (K760152) manufactured by Edwards Laboratories. 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 18, 1976. Regulation: 8.