510(k) Report

FDA applicant

Meps, LLC

Fort Lauderdale, FL1 decision2002–20020 recalls

FDA records 1 decision for Meps, LLC (Fort Lauderdale, FL) in 2002: 1 510(k) clearance. All are in product code GWF (Stimulator, Electrical, Evoked Response). 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 Meps, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Meps, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Meps, LLC 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?

  • GWFStimulator, Electrical, Evoked Response1decision

Who builds on its devices?

Later devices cite its devices 5 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.

  • K020400Digitimer D185 Multipulse Cortical StimulatorMeps, LLC · 20025cite it

What has FDA decided for it lately?

  • K020400Digitimer D185 Multipulse Cortical StimulatorMeps, LLC · 2002

The one decision as Meps, LLC →