VX4 RECORDING PULSE OXIMETER

VX4 RECORDING PULSE OXIMETER is an FDA 510(k)-cleared medical device (K935510) manufactured by Vitalog Monitoring,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 June 30, 1994. Regulation: 8.