
Riancorp Pty, Ltd.
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LTU-904 PORTABLE LASER THERAPY UNIT is an FDA 510(k)-cleared medical device (K030295) manufactured by Riancorp Pty, Ltd.. 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 December 22, 2004. Regulation: 8.