QUEST CORONARY SINUS PERFUSION CANNULA -FRCC

QUEST CORONARY SINUS PERFUSION CANNULA -FRCC is an FDA 510(k)-cleared medical device (K941916) manufactured by Quest Medical, 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 April 5, 1995. Regulation: 8.