MEDLINE STRIDER, MODELS MIDI 3 AND MIDI 4

MEDLINE STRIDER, MODELS MIDI 3 AND MIDI 4 is an FDA 510(k)-cleared medical device (K032446) manufactured by Medline Industries, 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 February 11, 2004. Regulation: 8.