CELSITE IMPLANTABLE PORT WITH VALVED CATHETER

CELSITE IMPLANTABLE PORT WITH VALVED CATHETER is an FDA 510(k)-cleared medical device (K993024) manufactured by B. Braun of America, Inc.. 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 March 12, 2000. Regulation: 8.