N.E.S.S. Nuromuscular Electrical Stimulation Syst is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
N.E.S.S. Nuromuscular Electrical Stimulation Syst - FDA 510(k) Cleare...
1
Total
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Cleared
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Denied
N.E.S.S. Nuromuscular Electrical Stimulation Syst has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by N.E.S.S. Nuromuscular Electrical Stimulation Syst Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - N.E.S.S. Nuromuscular Electrical Stimulation Syst
1 devices