510(k) Report

FDA applicant

National Medical Technology

Mchenry, IL4 decisions1979–19870 recalls

FDA records 4 decisions for National Medical Technology (Mchenry, IL) from 1979 to 1987: 4 510(k) clearances. Most are in product codes DRX (Electrode, Electrocardiograph) and ENZ (Telescope, Laryngeal-Bronchial). 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, ear, nose and throat panel, where it files most

How often FDA has decided National Medical Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for National Medical Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — National Medical Technology 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?

  • DRXElectrode, Electrocardiograph2decisions
  • ENZTelescope, Laryngeal-Bronchial1decision
  • EQNLaryngoscope, Nasopharyngoscope1decision

What has FDA decided for it lately?

  • K871668Biodan Type Comet ElectrodeNational Medical Technology · 1987
  • K861158S&W Type 888 ElectrodeNational Medical Technology · 1986
  • K830888Cool-Lite Fibercoptic Laryngeal ExamNational Medical Technology · 1983
  • K790845Dualume Laryngeal Examination TelescopeNational Medical Technology · 1979

All 4 as National Medical Technology →