510(k) Report

FDA applicant

Medical Equipment Device Specialists

San Juan Capistrano, CA6 decisions2003–20040 recalls

FDA records 6 decisions for Medical Equipment Device Specialists (San Juan Capistrano, CA) from 2003 to 2004: 6 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and IPF (Stimulator, Muscle, Powered). 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 Medical Equipment Device Specialists’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Equipment Device Specialists since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Equipment Device Specialists by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medical Equipment Device Specialists’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief4decisions
  • IPFStimulator, Muscle, Powered2decisions

What has FDA decided for it lately?

  • K040193Model GST-1Medical Equipment Device Specialists · 2004
  • K032055Meds-4-Inf+Medical Equipment Device Specialists · 2003
  • K023446Meds-3 Neuromuscular StimulatorMedical Equipment Device Specialists · 2003
  • K023435Meds-4 Neuromuscular StimulatorMedical Equipment Device Specialists · 2003
  • K023439Meds-4 Neuromuscular StimulatorMedical Equipment Device Specialists · 2003
  • K023443Meds-3 Neuromuscular StimulatorMedical Equipment Device Specialists · 2003

All 6 as Medical Equipment Device Specialists →