MODIFICATIONS TO ACS CORONARY GUIDING CATHETER W/T

MODIFICATIONS TO ACS CORONARY GUIDING CATHETER W/T is an FDA 510(k)-cleared medical device (K851574) manufactured by Advanced Cardiovascular Systems, 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 June 18, 1985. Regulation: 8.