
Meditech International, Inc.
Free shipping on orders over $99 · 30-day returns
LD-I 75 AND LD-I 200 is an FDA 510(k)-cleared medical device (K072551) manufactured by Meditech International, 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 1, 2008. Regulation: 8.