ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF

ANASTOMART(TM) CORONARY BYPASS GRAFT MARKERS/MODIF is an FDA 510(k)-cleared medical device (K922025) manufactured by Pioneering Technologies, 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 September 21, 1992. Regulation: 8.