6 FR FL POWERHOHN AND POWERLINE CATHETER

6 FR FL POWERHOHN AND POWERLINE CATHETER is an FDA 510(k)-cleared medical device (K051417) 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 June 29, 2005. Regulation: 8.