MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI

MINOLTA PULSOX-3SI, PULSOX-3IA, PULSOX-3LI is an FDA 510(k)-cleared medical device (K010413) manufactured by Konica Minolta Sensing, 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 August 1, 2001. Regulation: 8.