510(k) Report

FDA applicant

Electrophoresis Corp.

Mchenry, IL4 decisions1979–19800 recalls

FDA records 4 decisions for Electrophoresis Corp. (Mchenry, IL) from 1979 to 1980: 4 510(k) clearances. Most are in product codes JJN (Apparatus, Electrophoresis, For Clinical Use) and JHY (Colorimetric Method, Cpk Or Isoenzymes). 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, clinical chemistry panel, where it files most

How often FDA has decided Electrophoresis Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electrophoresis Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Electrophoresis Corp. 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?

  • JJNApparatus, Electrophoresis, For Clinical Use1decision
  • JHYColorimetric Method, Cpk Or Isoenzymes1decision
  • GGMControl, Hemoglobin1decision
  • CFEElectrophoretic, Lactate Dehydrogenase Isoenzymes1decision

What has FDA decided for it lately?

  • K802395Special Procedure Aqarose FilmElectrophoresis Corp. · 1980
  • K790309CPK Isoenzyme SubstrateElectrophoresis Corp. · 1979
  • K790310Hemoglobin ControlsElectrophoresis Corp. · 1979
  • K790311LDH Isoenzyme ReagentElectrophoresis Corp. · 1979

All 4 as Electrophoresis Corp. →

Other applicant names beginning “Electrophoresis”

FDA records each applicant name separately; these may or may not be the same firm.

Electrophoresis Corp. of America 27