TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER

TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER is an FDA 510(k)-cleared medical device (K884375) manufactured by Argon Medical 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 January 10, 1989. Regulation: 8.