BURDICK 200 PULSE OXIMETER

BURDICK 200 PULSE OXIMETER is an FDA 510(k)-cleared medical device (K954267) manufactured by Burdick, 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 May 2, 1996. Regulation: 8.