MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE

MIDWESTERN REPROCESSING CENTER REPROCESSED PULSE OXIMETER PROBE is an FDA 510(k)-cleared medical device (K101280) manufactured by Midwest Reprocessing Center, LLC. 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 6, 2010. Regulation: 8.