Bard Power-Injectable Implantable Ports (PowerPorts®)

Bard Power-Injectable Implantable Ports (PowerPorts®) is an FDA 510(k)-cleared medical device (K181446) 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 July 7, 2019. Regulation: 8.