510(k) Report

FDA applicant

N.E.S.S. Nuromuscular Electrical Stimulation Syst

Washington, DC1 decision1998–19980 recalls

FDA records 1 decision for N.E.S.S. Nuromuscular Electrical Stimulation Syst (Washington, DC) in 1998: 1 510(k) clearance. All are in product code IPF (Stimulator, Muscle, Powered). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided N.E.S.S. Nuromuscular Electrical Stimulation Syst’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for N.E.S.S. Nuromuscular Electrical Stimulation Syst since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — N.E.S.S. Nuromuscular Electrical Stimulation Syst by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IPFStimulator, Muscle, Powered1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K982482Handmaster NMS1N.E.S.S. Nuromuscular Electrical Stimulation Syst · 19983cite it

What has FDA decided for it lately?

  • K982482Handmaster NMS1N.E.S.S. Nuromuscular Electrical Stimulation Syst · 1998

The one decision as N.E.S.S. Nuromuscular Electrical Stimulation Syst →

Other applicant names beginning “N.E.S.S.”

FDA records each applicant name separately; these may or may not be the same firm.

Ness-Neuromuscular Electrical Stimulation Systems 7