HORIZON 2000 TRANSCUTANEOUS GAS MONITORING

HORIZON 2000 TRANSCUTANEOUS GAS MONITORING is an FDA 510(k)-cleared medical device (K860124) manufactured by Mennen Medical, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 8, 1986. Regulation: 8.