POWERHICKMAN LONG-TERM INTRAVASCULAR CATHETER

POWERHICKMAN LONG-TERM INTRAVASCULAR CATHETER is an FDA 510(k)-cleared medical device (K061179) manufactured by C.R. Bard, 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 August 8, 2006. Regulation: 8.