CEFAR REHAB 2 AND REHAB 2 PRO

CEFAR REHAB 2 AND REHAB 2 PRO is an FDA 510(k)-cleared medical device (K030403) manufactured by Cefar Medical AB. 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 July 16, 2003. Regulation: 8.