510(k) Report

FDA applicant

Dr. John D. Reid B.A., D.C.

Mchenry, IL2 decisions1982–19830 recalls

FDA records 2 decisions for Dr. John D. Reid B.A., D.C. (Mchenry, IL) from 1982 to 1983: 2 510(k) clearances. All are in product code KYA (System, Thermographic, Liquid Crystal…). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Dr. John D. Reid B.A., D.C.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dr. John D. Reid B.A., D.C. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dr. John D. Reid B.A., D.C. 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?

  • KYASystem, Thermographic, Liquid Crystal, Nonpowered (Adjunctive Use)1decision

What has FDA decided for it lately?

  • K837100Digitizing Colorizing Apple Computer System for RE-View of Normal Roentgen FilmDr. John D. Reid B.A., D.C. · 1983
  • K821524Chiropratic Infra-Red Crystal PakDr. John D. Reid B.A., D.C. · 1982

All 2 as Dr. John D. Reid B.A., D.C. →