PS-41 6M PATIENT SIMULATOR

PS-41 6M PATIENT SIMULATOR is an FDA 510(k)-cleared medical device (K963198) manufactured by Metron U.S., 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 4, 1997. Regulation: 8.