CURITY(R) PERCUTANEOUS CATHETERS

CURITY(R) PERCUTANEOUS CATHETERS is an FDA 510(k)-cleared medical device (K895972) manufactured by Kendall Healthcare Products Co. Div.Of Tyco Health. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 1990. Regulation: 8.