TDX SP2 POWER WHEECHAIR

TDX SP2 POWER WHEECHAIR is an FDA 510(k)-cleared medical device (K141783) manufactured by Invacare Corporation. 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 January 8, 2015. Regulation: 8.