SPYGLASS 5 FR ANGIOGRAPHIC CATHETER

SPYGLASS 5 FR ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K982299) manufactured by Daig 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 October 18, 1998. Regulation: 8.