510(k) Report

FDA applicant

Neurotron, Inc.

Baltimore, MD2 decisions1985–19860 recalls

FDA records 2 decisions for Neurotron, Inc. (Baltimore, MD) from 1985 to 1986: 2 510(k) clearances. Most are in product codes LLN (Device, Vibration Threshold Measurement) and JXE (Device, Nerve Conduction Velocity Measurement). 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, neurology panel, where it files most

How often FDA has decided Neurotron, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neurotron, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Neurotron, 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?

  • LLNDevice, Vibration Threshold Measurement1decision
  • JXEDevice, Nerve Conduction Velocity Measurement1decision

Who builds on its devices?

Later devices cite its devices 6 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.

  • K853608NeurometerNeurotron, Inc. · 19864cite it
  • K843924Digital Electroneurometer S-100Neurotron, Inc. · 19852cite it

What has FDA decided for it lately?

  • K853608NeurometerNeurotron, Inc. · 1986
  • K843924Digital Electroneurometer S-100Neurotron, Inc. · 1985

All 2 as Neurotron, Inc. →

Other applicant names beginning “Neurotron”

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

Neurotron Medical 3