RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORING

RMI AORTIC ROOT/CORONARY SINUS PRESSURE MONITORING is an FDA 510(k)-cleared medical device (K897137) manufactured by Research 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 March 26, 1990. Regulation: 8.