SPOT CHECK PULSE OXIMETER,512/513

SPOT CHECK PULSE OXIMETER,512/513 is an FDA 510(k)-cleared medical device (K032949) manufactured by Respironics Novametrix, 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 22, 2004. Regulation: 8.