OHMEDA 3800 PULSE OXIMETER

OHMEDA 3800 PULSE OXIMETER is an FDA 510(k)-cleared medical device (K962127) manufactured by Ohmeda Medical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 9, 1996. Regulation: 8.