SHERPA SHERPA II AND ASCENT CORONARY GUIDING CATHETERS

SHERPA SHERPA II AND ASCENT CORONARY GUIDING CATHETERS is an FDA 510(k)-cleared medical device (K944668) manufactured by Medtronics Interventional Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 2, 1995. Regulation: 8.