MEDSIM 300 PATIENT SIMULATOR

MEDSIM 300 PATIENT SIMULATOR is an FDA 510(k)-cleared medical device (K935817) manufactured by Dynatech/Nevada, 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 January 17, 1994. Regulation: 8.