CURITY PERCUTANEOUS CATHETER INSERTION KIT

CURITY PERCUTANEOUS CATHETER INSERTION KIT is an FDA 510(k)-cleared medical device (K855061) manufactured by The Kendal Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 15, 1986. Regulation: 8.