REPROCESSED PULSE OXIMETER SENSORS

REPROCESSED PULSE OXIMETER SENSORS is an FDA 510(k)-cleared medical device (K012677) manufactured by Sterilmed, 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 March 27, 2003. Regulation: 8.