MONAGHAN RVM, MODEL 760 AND 761

MONAGHAN RVM, MODEL 760 AND 761 is an FDA 510(k)-cleared medical device (K863612) manufactured by Monaghan Medical Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 14, 1986. Regulation: 8.