SIDEKICK and USHER Support Catheters

SIDEKICK and USHER Support Catheters is an FDA 510(k)-cleared medical device (K161986) manufactured by Bard Peripheral Vascular, 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 3, 2016. Regulation: 8.