ROMFLEX REHAB EQUIP EXTREMITIES UNIT

ROMFLEX REHAB EQUIP EXTREMITIES UNIT is an FDA 510(k)-cleared medical device (K910150) manufactured by Dyna Flex, Intl.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 22, 1991. Regulation: 8.