HORIZON 2000 PULSE OXIMETRY AND MODULE

HORIZON 2000 PULSE OXIMETRY AND MODULE is an FDA 510(k)-cleared medical device (K882273) manufactured by Mennen Medical, 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 August 24, 1988. Regulation: 8.