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Restorative Therapies, Inc.
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RT300-S, MODEL FA100052, RT300-SP (PEDIATRIC VERSION), MODEL FA100053 is an FDA 510(k)-cleared medical device (K071113) 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 July 4, 2007. Regulation: 8.