CONMED PRO2 PULSE REFLECTANCE OXIMETER, MODEL PRO-M

CONMED PRO2 PULSE REFLECTANCE OXIMETER, MODEL PRO-M is an FDA 510(k)-cleared medical device (K061112) manufactured by Conmed Corporation. 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 21, 2006. Regulation: 8.