FINGER PULSE OXIMETER, MODEL 9560

FINGER PULSE OXIMETER, MODEL 9560 is an FDA 510(k)-cleared medical device (K081285) manufactured by Nonin Medical, 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 4, 2008. Regulation: 8.