FILTERSET W/Y-INJECTION SITE, 0.2

FILTERSET W/Y-INJECTION SITE, 0.2 is an FDA 510(k)-cleared medical device (K772312) manufactured by Abbott Laboratories. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 1978. Regulation: 8.