
Restorative Therapies, Inc.
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RT300-SL, MODEL FA100052; RT300-SLSA, MODEL FA104581 is an FDA 510(k)-cleared medical device (K090750) manufactured by Restorative Therapies, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 2009. Regulation: 8.