Ness-Neuromuscular Electrical Stimulation Systems - FDA 510(k) Cleare...
Recent clearances: NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT, MODIFICATION TO:NESS L300, NESS L300
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Cleared
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Denied
FDA 510(k) Regulatory Record - Ness-Neuromuscular Electrical Stimulation Systems Physical Medicine ✕
2 devices