QUINTON MEDTRACK CR PLUS TREADMILL

QUINTON MEDTRACK CR PLUS TREADMILL is an FDA 510(k)-cleared medical device (K990866) manufactured by Quinton, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 28, 1999. Regulation: 8.