SIDEKICK AND USHER SUPPORT CATHETERS

SIDEKICK AND USHER SUPPORT CATHETERS is an FDA 510(k)-cleared medical device (K131493) manufactured by C.R. Bard, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 1, 2013. Regulation: 8.