MONITOR, PATIENT, MODEL PM-I0N

MONITOR, PATIENT, MODEL PM-I0N is an FDA 510(k)-cleared medical device (K770968) manufactured by Cavitron 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 June 7, 1977. Regulation: 8.