
Restorative Therapies, Inc.
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RT300-S AND RT300-SP FES CYCLE ERGOMETER is an FDA 510(k)-cleared medical device (K072398) 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 November 20, 2007. Regulation: 8.