TORAY ANTHRON ANGIOGRAPHIC CATHETERS

TORAY ANTHRON ANGIOGRAPHIC CATHETERS is an FDA 510(k)-cleared medical device (K872983) manufactured by Toray Industries (America), 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 November 19, 1987. Regulation: 8.