510(k) Report

FDA applicant

Calnor of EL Paseo, Inc.

Mchenry, IL6 decisions1977–19840 recalls

FDA records 6 decisions for Calnor of EL Paseo, Inc. (Mchenry, IL) from 1977 to 1984: 6 510(k) clearances. Most are in product codes HCC (Device, Biofeedback) and FLE (Sterilizer, Steam). 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 Calnor of EL Paseo, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Calnor of EL Paseo, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Calnor of EL Paseo, 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?

  • HCCDevice, Biofeedback5decisions
  • FLESterilizer, Steam1decision

What has FDA decided for it lately?

  • K842354Emg Model 133Calnor of EL Paseo, Inc. · 1984
  • K841895GSR, 126, Eeg 130-Temp. 132, Emg 133Calnor of EL Paseo, Inc. · 1984
  • K842288EEG 130Calnor of EL Paseo, Inc. · 1984
  • K842353Temperature 132Calnor of EL Paseo, Inc. · 1984
  • K834152Ethylene Oxide Detector GLD-1-07Calnor of EL Paseo, Inc. · 1984
  • K771577Clinical Emg Model 133Calnor of EL Paseo, Inc. · 1977

All 6 as Calnor of EL Paseo, Inc. →