
Meditech International, Inc.
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BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS is an FDA 510(k)-cleared medical device (K041885) 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 February 23, 2005. Regulation: 8.