VANGUARD REPROCESSED PULSE OXIMETER SENSORS

VANGUARD REPROCESSED PULSE OXIMETER SENSORS is an FDA 510(k)-cleared medical device (K012344) manufactured by Vanguard Medical Concepts, 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 October 3, 2002. Regulation: 8.