MODIFIED NOVOSTE ANGIOGRAPHIC CATHETER

MODIFIED NOVOSTE ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K900460) manufactured by Novoste Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 16, 1990. Regulation: 8.