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Rehabilitative Resources, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K921323 CERVICAL PASSIVE MOTIONBXB1992-06-03 View
510(k) K920519 LUMBAR CPMBXB1992-03-13 View
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