FDA 510(k), K052289, DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE

FDA 510(k), K052289, DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE

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510(K) Number: K052289
Device Name: DEEPWAVE NEUROMODULATION PAIN THERAPY DEVICE
Manufacturer:
Device Classification Name: Interferential Current Therapy
Regulation Number: 882.5890
Classification Product Code: LIH
Date Received: 08/23/2005
Decision Date: 12/13/2005
Regulation Medical Specialty: Neurology
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