ROMFLEX REHAB EQUIP LATERAL FLEXION UNIT

ROMFLEX REHAB EQUIP LATERAL FLEXION UNIT is an FDA 510(k)-cleared medical device (K910149) 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 17, 1991. Regulation: 8.