RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE

RMI AORTIC ROOT PRESSURE MONITOR EXTENSION LINE is an FDA 510(k)-cleared medical device (K896777) 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 February 26, 1990. Regulation: 8.