510(k) Report

FDA applicant

Neurotech, Inc.

Washington, DC3 decisions1986–19960 recalls

FDA records 3 decisions for Neurotech, Inc. (Washington, DC) from 1986 to 1996: 3 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Neurotech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neurotech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Neurotech, Inc. 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, Powered2decisions
  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K860315Neurotech-16 Program System Controller Model 280Neurotech, Inc. · 19861cites it

What has FDA decided for it lately?

  • K955470Action Potential Simulation Therapy DeviceNeurotech, Inc. · 1996
  • K860315Neurotech-16 Program System Controller Model 280Neurotech, Inc. · 1986
  • K860314Neurotech-4 Program Neuromuscular Stimulator 281Neurotech, Inc. · 1986

All 3 as Neurotech, Inc. →