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Dyna Flex, Intl.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K910150 ROMFLEX REHAB EQUIP EXTREMITIES UNITBXB1991-01-23 View
510(k) K910149 ROMFLEX REHAB EQUIP LATERAL FLEXION UNITBXB1991-01-18 View
510(k) K910151 ROMFLEX REHAB EQUIP CERVICAL FLEXOR UNITBXB1991-01-18 View
510(k) K905299 ROMFLEX REHABILITATION EQUIPMENTBXB1990-12-31 View
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